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Multiple Epidermal Growth Factor-like Domains 8

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includes a supplementary data set that shows a multiple sequence alignment of the regions surrounding the SNPs and the domain in which the SNP lies. The Gly199 to Arg mutation is located inside an EGF-domain; the Arg1499 to His mutation is located within a kelch domain in the 7-bladed beta-sheet propeller; the Ser2367 to Gly is located within an EGF-Laminin domain. These domain are important to maintaining a properly folded protein and its function.
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text-mining in STRING. Together, it is with reasonably high confidence that the proteins in red are interacting with MEGF8, and with moderate confidence that the proteins in green interact with MEGF8. The confidence level for the proteins in blue is much lower, which may mean that the two-hybrid assay provided a false positive, or that they actually are interacting.
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amino acid bias was able to be determined. Isoform one is rich in cysteine and glycine, and deficient in isoleucine and lysine. Isoform 2 of MEGF8 was found to have very high levels of cysteine, moderately high levels of glycine, and low levels of isoleucine and lysine. The high levels of cysteine residues contributes to the numerous
1769:: laminins are the major noncollagenous components of basement membranes that mediate cell adhesion, growth migration, and differentiation; the laminin-type epidermal growth factor-like module occurs in tandem arrays; the domain contains 4 disulfide bonds (loops a-d) the first three resemble epidermal growth factor (EGF). 2193:. This GeoProfile also indicated that MEGF8 was found to be at moderate to moderately low expression levels in all other tissues examined. NCBI GeoProfile data also provided the tissue expression graph for MEGF8 in humans, which is displayed to the right, further illustrating specific sites and levels of expression 2594:
part of the D1k3ia3 structural domain remains in exon 29, but the kelch repeat has been excised, which could lead to structural issues. Also this variant contains almost 3 PSI domains, and an area of low complexity in exons 32-35, which may allow this variant to function in the cell, but no signal or
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in humans (19q13.2). There are two isoform constructs known for MEGF8, which differ by a 67 amino acid indel. The isoform 2 splice version (analyzed throughout this page) is 2785 amino acids long, and predicted to be 296.6 kdal in mass. Isoform 1 is composed of 2845 amino acids and predicted to weigh
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super family. Each of the seven blades are made up of a four stranded beta-folded motifs. It is also important to note that although many phosphorylation sites are predicted at high confidence, several other topographic predictions (i.e. disulfide bonds, glycosylation, other extracellular features),
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MEGF8 has one known paralog: ATRNL1. The ATRNL1 protein is approximately half the length of MEGF8, and contains several of the same conserved domains, including the CUB domain and transmembrane sequence. It is key to note that ATRNL1 is found in many birds and amphibians, where MEGF8 is not found in
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Spliced out exons 1-6; these exons hold several key domains and motifs including the CUB domain, two PSI domains, a D1k3ia3 structural domain, and a kelch repeat. This may result in a misfolded protein without the structural segments, and inhibit participation in development events (loss of PSI and
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Prediction software PELE from UCSC Biology Workbench indicated that MEGF8 is primarily composed of beta-folded sheets, with occasional short alpha helix segments. PELE uses eight different prediction programs to compare and confirm predictions, enhancing the confidence level. The beta-folded sheets
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The promoter having promoter ID number GXP_1262882 and transcript ID GXT_22531930, was predicted with the highest confidence. This promoter is located on the plus strand of chromosome 19, ranging from nucleotide 42829077 to 42830497, making it a 1421 nucleotide long sequence. The promoter sequence
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has spliced out Exon 13. Looking at the attached working conceptual translation, it can be seen that exon 3 does not code for any feature, domain, motif or other functional section of aa, and is likely therefore not key to the function of MEGF8 protein. This is the variant that corresponds to the
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found in the mature protein's folded structure. Overall, MEGF8 has a pH between 6.4 and 7.0, depending on the organism's sequence. Human MEGF8's pH is 6.4. This nearly neutral pH enables the protein to fold properly and inhibits denaturation. The twenty most conserved amino acids, found through a
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MEGF8 is composed of either 2845 amino acids (Isoform 1) or 2778 amino acids (Isoform 2). Isoform 2 undergoes a 67 amino acid removal from 700-766, which accounts for its shortened length; otherwise, the two isoforms are identical. Using SAPS, a Statistical Analysis of Protein Sequence software,
1750:: Calcium-binding EGF-like domain, present in a large number of membrane-bound and extracellular (mostly animal) proteins. Many of these proteins require calcium for their biological function and calcium-binding sites have been found to be located at the N-terminus of particular EGF-like domains. 3064:
Marchler-Bauer A, Lu S, Anderson JB, Chitsaz F, Derbyshire MK, DeWeese-Scott C, Fong JH, Geer LY, Geer RC, Gonzales NR, Gwadz M, Hurwitz DI, Jackson JD, Ke Z, Lanczycki CJ, Lu F, Marchler GH, Mullokandov M, Omelchenko MV, Robertson CL, Song JS, Thanki N, Yamashita RA, Zhang D, Zhang N, Zheng C,
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A fairly highly conserved protein, MEGF8 has conserved orthologs from P. paniscus to N. vectensis. Orthologs are found in mammals, amphibians, fish, insects, crustaceans, and invertebrates. Organization of the data showed that as time since divergence between humans and orthologs increased, the
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There are several SNPs, found through NCBI GeneView, that cause missense or silent mutations in MEGF8. However, three SNP mutations were identified as causes of Carpenter Syndrome 2 by Twigg et al. The three SNP mutations are: Gly199 to Arg; Arg1499 to His; Ser2367 to Gly. The article by Twigg
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searches, orthologs were found primarily in mammals, but MEGF8 is also conserved in invertebrates and fishes, and rarely in birds, reptiles, and amphibians. A notably important paralog to multiple epidermal growth factor-like domains 8 is ATRNL1 (Attractin-like 1), which is also a single pass
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In the table below, all predicted interactions, except SMARCD3, are supported by two-hybrid screen experimental data. This information is supported by both NextProt database and IntAct database. The two interactions with the highest confidence value are also supported by materials found by
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MEGF8 is predicted to contain several different types of features, domains, and motifs that play a key role in the protein's function, structure, and location. These are listed in Table 1. Functions, found through SMART analysis, as well as NCBI Conserved Domains Search include:
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Kerrien S, Aranda B, Breuza L, Bridge A, Broackes-Carter F, Chen C, Duesbury M, Dumousseau M, Feuermann M, Hinz U, Jandrasits C, Jimenez RC, Khadake J, Mahadevan U, Masson P, Pedruzzi I, Pfeiffenberger E, Porras P, Raghunath A, Roechert B, Orchard S, Hermjakob H (January 2012).
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This variant is exons 36-40, excised 41, and a shortened 42 exon. It possesses EGF calcium domains and EGF/EGF-like domains. Loss of 41 will drastically alter the function as it possesses the TMEM segment. It depends on where 41 is lost and 42 is cleaved.
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Mediates the entry of calcium ions into excitable cells and are also involved in a variety of calcium-dependent processes, including muscle contraction, hormone or neurotransmitter release, gene expression, cell motility, cell division and cell
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There is no research being done currently to develop treatment or cures for Carpenter Syndrome 2. Researchers are still striving to understand the cause of the point mutations in MEGF8 that result in this extremely rare genetic disease.
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located in Heidelberg, Germany. MEGF8 has been predicted to be a key player in several developmental processes, such as left-right patterning and limb formation. Currently, researchers have found MEGF8 SNP mutations to be the cause of
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Essential proto-oncogenic transcriptional regulator; Transcriptional repressor or activator depending on both promoter and cell type context; represses promoter activity of SOCS1 and SOCS3 and thus, may regulate cytokine signaling
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Zhang Z, Alpert D, Francis R, Chatterjee B, Yu Q, Tansey T, Sabol SL, Cui C, Bai Y, Koriabine M, Yoshinaga Y, Cheng JF, Chen F, Martin J, Schackwitz W, Gunn TM, Kramer KL, De Jong PJ, Pennacchio LA, Lo CW (March 2009).
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Zhang Z, Alpert D, Francis R, Chatterjee B, Yu Q, Tansey T, Sabol SL, Cui C, Bai Y, Koriabine M, Yoshinaga Y, Cheng JF, Chen F, Martin J, Schackwitz W, Gunn TM, Kramer KL, De Jong PJ, Pennacchio LA, Lo CW (March 2009).
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Mutations in MEGF8 have been found to be linked to defective lateralization during development, as reported by Twigg et al. Common features of individuals with Carpenter Syndrome Subtype II include the following:
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Acts as component of the STAGA transcription coactivator-HAT complex. Mediates the interaction of STAGA complex with the CRX and is involved in CRX-dependent gene activation. Necessary for microtubule cytoskeleton
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occur at many of the key domains, including the EGF-domains, kelch domains, and EGF-laminin domains. This information from PELE also corresponded with the secondary structure and 3D structure predictions made by
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are involved in the development of neural and epithelial tissues; semaphorins induce the collapse and paralysis of neuronal growth cones; and integrins may mediate adhesive or migratory functions of epithelial
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Twigg SR, Lloyd D, Jenkins D, Elçioglu NE, Cooper CD, Al-Sannaa N, Annagür A, Gillessen-Kaesbach G, Hüning I, Knight SJ, Goodship JA, Keavney BD, Beales PL, Gileadi O, McGowan SJ, Wilkie AO (November 2012).
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Twigg SR, Lloyd D, Jenkins D, Elçioglu NE, Cooper CD, Al-Sannaa N, Annagür A, Gillessen-Kaesbach G, Hüning I, Knight SJ, Goodship JA, Keavney BD, Beales PL, Gileadi O, McGowan SJ, Wilkie AO (November 2012).
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Cohen DM, Green JG, Miller J, Gorlin RJ, Reed JA (October 1987). "Acrocephalopolysyndactyly type II--Carpenter syndrome: clinical spectrum and an attempt at unification with Goodman and Summit syndromes".
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Barrett T, Troup DB, Wilhite SE, Ledoux P, Evangelista C, Kim IF, Tomashevsky M, Marshall KA, Phillippy KH, Sherman PM, Muertter RN, Holko M, Ayanbule O, Yefanov A, Soboleva A (January 2011).
1062:, is a protein coding gene that encodes a single pass membrane protein, known to participate in developmental regulation and cellular communication. It is located on chromosome 19 at the 49th 3971:
Victorine AS, Weida J, Hines KA, Robinson B, Torres-Martinez W, Weaver DD (March 2014). "Prenatal diagnosis of Carpenter syndrome: looking beyond craniosynostosis and polysyndactyly".
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Nakayama M, Nakajima D, Nagase T, Nomura N, Seki N, Ohara O (July 1998). "Identification of high-molecular-weight proteins with multiple EGF-like motifs by motif-trap screening".
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Epidermal Growth Factor Domain: a short peptide with a distinctive motif of six cysteines, which is found in many different proteins of diverse functions
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for more extensive details related to the disease. Genetic mutations in MEGF8 have been found to be a principal cause of this rare genetic syndrome.
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Analysis of gene ontology information by BioGPS was able to produce a list of biological processes in each of which MEGF8 plays a significant role:
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Nakai K, Horton P (January 1999). "PSORT: a program for detecting sorting signals in proteins and predicting their subcellular localization".
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Frias JL, Felman AH, Rosenbloom AL, Finkelstein SN, Hoyt WF, Hall BD (1978). "Normal intelligence in two children with Carpenter syndrome".
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Lane L, Argoud-Puy G, Britan A, Cusin I, Duek PD, Evalet O, Gateau A, Gaudet P, Gleizes A, Masselot A, Zwahlen C, Bairoch A (January 2012).
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Jensen LJ, Kuhn M, Stark M, Chaffron S, Creevey C, Muller J, Doerks T, Julien P, Roth A, Simonovic M, Bork P, von Mering C (January 2009).
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According to BioGPS gene ontology information, MEGF8 is an active participant in receptor activity, calcium ion binding, protein binding.
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Blom N, Gammeltoft S, Brunak S (December 1999). "Sequence and structure-based prediction of eukaryotic protein phosphorylation sites".
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Plays a role in ATP dependent nucleosome remodeling by SMARCA4 containing complexes. Stimulates nuclear receptor mediated transcription
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Transcriptional corepressor. Recruits NR2E1 to repress transcription. Promotes vascular smooth cell (VSMC) migration and orientation
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Activator-, mediator- and TBP-dependent core promoter element for RNA polymerase II transcription from TATA-less promoters
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The four primary splice variants and their distinctions are described below (labels correspond to those in image below):
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MEGF8 is found to be expressed at high levels in cardiac myocytes and fetal brain tissue, according to GeoProfiles, from
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Bendtsen JD, Nielsen H, von Heijne G, Brunak S (July 2004). "Improved prediction of signal peptides: SignalP 3.0".
1318: 1743:: contains several sub-families of different functions according to location and protein; not specified for MEGF8. 265: 164: 1756:: Galactose oxidase, central domain; Found to cause formation of ß propeller tertiary structure of the protein. 1384: 829: 83: 3578:
Wu C, Orozco C, Boyer J, Leglise M, Goodale J, Batalov S, Hodge CL, Haase J, Janes J, Huss JW, Su AI (2009).
3361:"Prediction of post-translational glycosylation and phosphorylation of proteins from the amino acid sequence" 4238: 4008:
Engelhard C, Sarsfield S, Merte J, Wang Q, Li P, Beppu H, Kolodkin AL, Sucov HM, Ginty DD (September 2013).
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promoter region through Genomatix. The top twenty most confidently predicted factors include the following:
1230: 810: 66:, C19orf49, CRPT2, EGFL4, SBP1, Multiple Epidermal Growth Factor-like Domains 8, multiple EGF like domains 8 2196: 510: 3415: 1560: 1428: 1068: 147: 2105:
56; 223; 267; 427; 699; 749; 968; 987; 1054; 1140; 1210; 1539; 1908; 1929; 2006; 2153; 2168; 2340; 2778
1601: 4172:"Massively parallel sequencing identifies the gene Megf8 with ENU-induced mutation causing heterotaxy" 2789:"Massively parallel sequencing identifies the gene Megf8 with ENU-induced mutation causing heterotaxy" 1959: 4183: 3580:"BioGPS: an extensible and customizable portal for querying and organizing gene annotation resources" 3453:"Advantages of combined transmembrane topology and signal peptide prediction--the Phobius web server" 2888: 2800: 3420: 2605: 62: 1186: 979: 954: 928: 903: 1142: 1072:
transmembrane protein, with several of the same key features and motifs as MEGF8, as indicated by
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SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily d, member (
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This diagram from AceView depicts the various forms of MEGF8 produced by alternative splicing
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More than one hundred transcription factor binding sites were predicted to be found in the
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Andreeva A, Howorth D, Chandonia JM, Brenner SE, Hubbard TJ, Chothia C, Murzin AG (2008).
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241-276; 340-388; 454-504; 519-575; 1450-1492; 1505-1552; 1724-1764; 1780-1820; 2239-2255
1766: 1747: 1740: 1698: 1605: 1450: 327: 2877:"SMART, a simple modular architecture research tool: identification of signaling domains" 4187: 3730:"STRING 8--a global view on proteins and their functional interactions in 630 organisms" 3274:
Gramatikoff K, et al. (2004). "In Frontiers of Biotechnology and Pharmaceuticals".
2892: 2804: 4206: 4171: 4152: 4127: 4108: 4083: 4036: 4009: 3861: 3836: 3806: 3781: 3754: 3729: 3705: 3680: 3655: 3630: 3606: 3579: 3552: 3527: 3477: 3452: 3251: 3226: 3202: 3177: 3091: 2823: 2788: 2672: 1981: 1759: 1734:: extracellular domain: present in proteins mostly known to be involved in development. 1472: 3154: 699: 694: 689: 684: 679: 674: 669: 664: 659: 654: 649: 644: 639: 634: 629: 624: 619: 614: 609: 604: 588: 583: 578: 573: 557: 552: 4227: 3337: 2911: 2876: 1516: 539: 3392: 2007:
Table 3: Key Predicted Post Translational Modifications Found in MEGF8 Human Protein
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Karlin S (June 1995). "Statistical significance of sequence patterns in proteins".
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Table 2: Predicted Key Features, Domains, & Motifs Found in MEGF8 Human Protein
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National Center for Biotechnology Information, U.S. National Library of Medicine
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National Center for Biotechnology Information, U.S. National Library of Medicine
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of 20 orthologs, were found to be located in the CUB and transmembrane domains.
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Proceedings of the National Academy of Sciences of the United States of America
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Proceedings of the National Academy of Sciences of the United States of America
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Proceedings of the National Academy of Sciences of the United States of America
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positive regulation of axon extension involved in axon guidance (GO:0048842)
1608:), a gene promoter database, predicted ten different possible promoters for 729: 488: 366: 311: 298: 210: 197: 99: 4215: 4161: 4117: 4066: 4045: 3992: 3870: 3815: 3763: 3714: 3664: 3615: 3561: 3486: 3437: 3384: 3376: 3310: 3302: 3260: 3211: 3162: 3100: 3043: 3034: 2832: 2588:
CUB). Still has signal and TMEM so may still be able to partially function
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Davis CG (May 1990). "The many faces of epidermal growth factor repeats".
3082: 2934: 2920: 1992:. SCOP also indicated that the beta-propeller in MEGF8 is a member of the 1043: 1038: 3984: 3910: 3745: 3468: 3359:
Blom N, Sicheritz-Pontén T, Gupta R, Gammeltoft S, Brunak S (June 2004).
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for the Human MEGF8 Sequence, with the NCBI accession number BAA32469.2.
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One of the key attributes of MEGF8's tertiary structure is its 7-bladed
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epiboly involved in gastrulation with mouth forming second (GO:0055113)
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Chorion-specific transcription factors with a GCM DNA binding domain
3178:"Data growth and its impact on the SCOP database: new developments" 3528:"NCBI GEO: archive for functional genomics data sets--10 years on" 2604: 2414: 2355: 2263:
determination of digestive tract left/right asymmetry (GO:0071907)
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Calcium Channel, Voltage-Dependent, P/Q Type, Alpha 1A Subunit (
1762:: A motif found in regulatory proteins, as predicted by PSORT II 714: 710: 2385: 1988:
found in its D1k3ia3 structural domain, which was identified by
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EGR/nerve growth factor induced protein C & related factors
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positive regulation of axon extension involved in axon guidance
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embryonic heart tube left/right pattern formation (GO:0060971)
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148-177; 180-210; 1057-1100; 2121-2160; 2162-2190; 2200-2240
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787-839; 889-931; 945-1013; 1864-1919; 2008-2058; 2060-2117
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overlaps with the transcriptional start codon in the gene.
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epiboly involved in gastrulation with mouth forming second
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Alternative Splicing, Mutations, & Phenotypic Impacts
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is a growth factor independent 1B transcription repressor
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Ceroni A, Passerini A, Vullo A, Frasconi P (July 2006).
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Table 4: Putative Protein Interactions with Human MEGF8
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determination of heart left/right asymmetry (GO:0061371)
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NCBI GeoProfile for MEGF8 Tissues Expression in Humans
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Schultz J, Milpetz F, Bork P, Ponting CP (May 1998).
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determination of digestive tract left/right asymmetry
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embryonic skeletal system morphogenesis (GO:0048704)
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cell migration involved in gastrulation (GO:0042074)
3681:"The IntAct molecular interaction database in 2012" 3631:"neXtProt: a knowledge platform for human proteins" 2595:TMEM to place in membrane so not a normal function 1971:
Human ATRNL1 (Paralog to MEGF8) Protein Feature Map
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negative regulation of smoothened signaling pathway
3780:, Ostell J, Pruitt KD, Tatusova T (January 2011). 2729: 2727: 2725: 2708: 2706: 2704: 2269:fasciculation of sensory neuron axon (GO:0097155) 625:embryonic heart tube left/right pattern formation 282: 181: 3782:"Entrez Gene: gene-centered information at NCBI" 2963:. Department of Mathematics, Stanford University 1645:Signal transducer and activator of transcription 2666:Obesity in later life *congenital heart disease 2227:embryonic heart tube morphogenesis (GO:0003143) 1060:Multiple Epidermal Growth Factor-like Domains 8 27:Protein-coding gene in the species Homo sapiens 3926: 3924: 3922: 3920: 2734:GRCm38: Ensembl release 89: ENSMUSG00000045039 2266:craniofacial suture morphogenesis (GO:0097094) 2361:Two-Hybrid (IntAct) Text-mining (STRING/OMIM) 2205:Function and Mechanisms in Cellular Processes 8: 3973:American Journal of Medical Genetics. Part A 3451:Käll L, Krogh A, Sonnhammer EL (July 2007). 2713:GRCh38: Ensembl release 89: ENSG00000105429 1931:1103-1148; 1346-1485; 2244-2317; 2320-2381 615:determination of heart left/right asymmetry 2230:regulation of gene expression (GO:0010468) 2001:Predicted Post Translational Modifications 1963:Scaled Map of MEGF8 Features along protein 1660:Neuron-specific olfactory factor (2 sites) 725: 535: 323: 222: 119: 4205: 4195: 4151: 4107: 4035: 4025: 3860: 3805: 3753: 3704: 3654: 3605: 3595: 3551: 3476: 3419: 3250: 3201: 3090: 3033: 2910: 2900: 2853:. Weizmann Institute of Science in Israel 2822: 2812: 2257:left/right pattern formation (GO:0060972) 2233:embryonic limb morphogenesis (GO:0030326) 1806:Simple Modular Architecture Research Tool 1074:Simple Modular Architecture Research Tool 2700: 2413:Apinocerebellar ataxia type 7 protein ( 680:cell migration involved in gastrulation 605:embryonic skeletal system morphogenesis 2480:Text-mining (OMIM article for SMARCS3) 1794:Predicted Domain & Motif Locations 1633:Vertebrate TATA binding protein factor 31: 3326:Current Opinion in Structural Biology 1078:European Molecular Biology Laboratory 287: 248: 243: 186: 145: 140: 7: 4084:"BMP signaling in axon regeneration" 3934:American Journal of Medical Genetics 3891:American Journal of Medical Genetics 2581:splice model of the analyzed megf8. 2352:Found in Endothelial & Erythroid 1859:Epidermal Growth Factor (EGF) Domain 1722:Predicted Key Domains & Features 1672:Nuclear receptor subfamily 2 factors 685:fasciculation of sensory neuron axon 655:determination of left/right symmetry 459:vestibular membrane of cochlear duct 3008:, Sternberg MJ (26 February 2009). 2984:"PELE-Protein Structure Prediction" 2043:Cysteine involved in Disulfide Bond 1589:any birds, and only one amphibian. 4132:American Journal of Human Genetics 3841:American Journal of Human Genetics 2236:BMP signaling pathway (GO:0030509) 2029:Amino Acid Location Range (1-2785) 1997:do not support these predictions. 1830:Amino Acid Location Range (1-2785) 1681:Neuron-restrictive silencer factor 1657:KRAB domain zinc finger protein 57 969: 944: 918: 889: 865: 846: 820: 801: 775: 756: 665:embryonic heart tube morphogenesis 505: 423: 361: 340: 25: 650:craniofacial suture morphogenesis 2091:CQCNGH 1144-1149 & 2313-2318 640:coronary vasculature development 509: 271: 264: 258: 235: 170: 163: 157: 132: 40: 4088:Current Opinion in Neurobiology 2640:Adverse Phenotypic Consequences 2239:limb morphogenesis (GO:0035108) 1816:Feature, Domain, or Motif Name 1076:(SMART) which is hosted by the 4082:Zhong J, Zou H (August 2014). 3143:Trends in Biochemical Sciences 2295:Predicted Interacting Protein 1630:Ccaat/Enhancer Binding Protein 1209:Trichechus manatus latirostris 1099:sequence identity decreased. 574:integral component of membrane 520:More reference expression data 489:More reference expression data 405:right hemisphere of cerebellum 1: 3463:(Web Server issue): W429–32. 3237:(Web Server issue): W177–81. 3155:10.1016/S0968-0004(98)01336-X 2119:between amino acids 34 and 35 1772:PSI domain: domain found in 1666:RXR heterodimer binding sites 1539:Strongylocentrotus purpuratus 670:regulation of gene expression 256: 155: 4234:Genes on human chromosome 19 3538:(Database issue): D1005–10. 3408:Journal of Molecular Biology 3338:10.1016/0959-440X(95)80098-0 3291:Journal of Molecular Biology 2957:"Statistical Analysis of PS" 2218:Role in Biological Processes 1663:Nuclear respiratory factor 1 1648:Heat shock factors (2 sites) 675:left/right pattern formation 660:embryonic limb morphogenesis 3188:(Database issue): D419–25. 2450:Two Hybrid Assay, Pull-Down 2282: 2004: 1797: 1704:multiple sequence alignment 1101: 4255: 4144:10.1016/j.ajhg.2012.08.027 4100:10.1016/j.conb.2014.03.009 3853:10.1016/j.ajhg.2012.08.027 3740:(Database issue): D412–6. 3691:(Database issue): D841–6. 3641:(Database issue): D76–83. 3597:10.1186/gb-2009-10-11-r130 3077:(Database issue): D225–9. 3065:Bryant SH (January 2011). 1654:Estrogen response elements 1319:Alligator mississippiensis 695:animal organ morphogenesis 3792:(Database issue): D52–7. 3430:10.1016/j.jmb.2004.05.028 2769:"Mouse PubMed Reference:" 2751:"Human PubMed Reference:" 2368:IntAct, STRING, NextProt 2323:Experimental/Text Support 2022:Number Predicted in MEGF8 1804:Found through the use of 1094:Evolution & Orthologs 1042: 1037: 1033: 1026: 1010: 991: 976: 951: 940: 925: 896: 885: 872: 868: 853: 849: 840: 827: 823: 808: 804: 795: 782: 778: 763: 759: 750: 735: 728: 724: 708: 538: 534: 517: 508: 499: 486: 435: 426: 373: 364: 334: 326: 322: 305: 292: 255: 234: 225: 221: 204: 191: 154: 131: 122: 118: 73: 70: 60: 53: 48: 39: 34: 2986:. SDSC Biology Workbench 2052:DISULFIND & UniProt 1870:D1k3ia Structural Domain 1599:http://www.genomatix.de/ 1385:Neolamprologus brichardi 1104:Table 1: MEGF8 Orthologs 997:Chr 19: 42.33 – 42.38 Mb 463:Rostral migratory stream 389:tendon of biceps brachii 4197:10.1073/pnas.0813400106 3946:10.1002/ajmg.1320280208 3903:10.1002/ajmg.1320020210 2902:10.1073/pnas.95.11.5857 2814:10.1073/pnas.0813400106 2113:Signal Peptide Cleavage 1984:which is formed by the 1675:Octamer binding protein 1499:Mediterranean Fruit Fly 1231:Leptonychotes weddellii 1004:Chr 7: 25.02 – 25.07 Mb 467:external carotid artery 451:internal carotid artery 4067:10.1006/geno.1998.5341 3786:Nucleic Acids Research 3734:Nucleic Acids Research 3685:Nucleic Acids Research 3635:Nucleic Acids Research 3532:Nucleic Acids Research 3457:Nucleic Acids Research 3377:10.1002/pmic.200300771 3303:10.1006/jmbi.1999.3310 3231:Nucleic Acids Research 3182:Nucleic Acids Research 3071:Nucleic Acids Research 2610: 2201: 2099:N-linked Glycosylation 1972: 1964: 1892:Leucine Zipper Pattern 1597:Genomatix's ElDorado ( 1561:Nematostella vectensis 409:superior frontal gyrus 2660:Polysyndactyly Digits 2608: 2524:(Q8CKF8 in UniProtKB) 2440:Certain Brain Tissues 2420:Two Hybrid, Pull-Down 2275:Putative Interactions 2199: 2164:Phobius, SAPS, SMART 1970: 1962: 1651:GC-Box factors SP1/GC 1636:CCAAT binding factors 1617:Transcription Factors 645:BMP signaling pathway 584:extracellular exosome 397:primary visual cortex 377:middle temporal gyrus 148:Chromosome 19 (human) 3985:10.1002/ajmg.a.36362 3026:10.1038/nprot.2009.2 2650:Tower-shaped skull ( 2628:Carpenter Syndrome 2 2169:Intracellular Domain 2155:Transmembrane Region 2141:Extracellular Domain 1947:Transmembrane Region 1687:Protein Architecture 1669:GATA binding factors 1429:IIctalurus punctatus 1116:Organism Common Name 250:Chromosome 7 (mouse) 4188:2009PNAS..106.3219Z 4027:10.7554/eLife.01160 3798:10.1093/nar/gkq1237 3697:10.1093/nar/gkr1088 3647:10.1093/nar/gkr1179 3544:10.1093/nar/gkq1184 3083:10.1093/nar/gkq1189 2893:1998PNAS...95.5857S 2805:2009PNAS..106.3219Z 2410:Mod-High Everywhere 2289: 2009: 1876:233-550; 1449-1801 1810: 1710:Secondary Structure 1565:Starlet Sea Anemone 1367:Western clawed frog 1131:Sequence Similarity 1106: 1067:303.1 kdal. Using 553:calcium ion binding 3746:10.1093/nar/gkn760 3469:10.1093/nar/gkm256 3243:10.1093/nar/gkl266 3194:10.1093/nar/gkm993 2657:Mental Retardation 2634:Carpenter syndrome 2611: 2550:Two Hybrid Pooling 2527:Two Hybrid Pooling 2503:Two Hybrid Pooling 2427:Int Act, NextProt 2283: 2210:Molecular Function 2202: 2127:Hydrophobic Domain 2063:K886; K1681; K1737 2046:99+ Possible Sites 2005: 1976:Tertiary Structure 1973: 1965: 1798: 1604:2021-12-02 at the 1495:Ceratitis capitata 1455:Japanese Rice Fish 1363:Xenopus tropicalis 1341:Alligator sinensis 1323:American Alligator 1297:Ophiophagus hannah 1102: 1083:Carpenter syndrome 1064:open reading frame 830:ENSMUSG00000045039 700:tissue development 620:limb morphogenesis 598:Biological process 567:Cellular component 546:Molecular function 475:supraoptic nucleus 471:epithelium of lens 385:right frontal lobe 3116:The New Biologist 2663:High birth weight 2562: 2561: 2556:IntAct, NextProt 2533:IntAct, NextProt 2509:IntAct, NextProt 2457:IntAct, NextProt 2182: 2181: 1994:galactose oxidase 1957: 1956: 1809: 1692:Primary Structure 1581: 1580: 1543:Purple Sea Urchin 1521:Common Water Flea 1477:Western Honey Bee 1345:Chinese alligator 1253:Rattus norvegicus 1126:Sequence Identity 1053: 1052: 1049: 1048: 1022: 1021: 987: 986: 966: 965: 936: 935: 915: 914: 881: 880: 862: 861: 836: 835: 817: 816: 791: 790: 772: 771: 720: 719: 530: 529: 526: 525: 495: 494: 482: 481: 420: 419: 401:entorhinal cortex 381:prefrontal cortex 318: 317: 217: 216: 112:MEGF8 - orthologs 16:(Redirected from 4246: 4219: 4209: 4199: 4165: 4155: 4121: 4111: 4078: 4049: 4039: 4029: 4004: 3958: 3957: 3928: 3915: 3914: 3886: 3875: 3874: 3864: 3831: 3820: 3819: 3809: 3774: 3768: 3767: 3757: 3725: 3719: 3718: 3708: 3675: 3669: 3668: 3658: 3626: 3620: 3619: 3609: 3599: 3575: 3566: 3565: 3555: 3523: 3517: 3516: 3514: 3512: 3497: 3491: 3490: 3480: 3448: 3442: 3441: 3423: 3403: 3397: 3396: 3356: 3350: 3349: 3321: 3315: 3314: 3286: 3280: 3279: 3271: 3265: 3264: 3254: 3222: 3216: 3215: 3205: 3173: 3167: 3166: 3138: 3132: 3131: 3111: 3105: 3104: 3094: 3061: 3055: 3054: 3052: 3050: 3037: 3014:Nature Protocols 3002: 2996: 2995: 2993: 2991: 2979: 2973: 2972: 2970: 2968: 2952: 2946: 2945: 2943: 2941: 2931: 2925: 2924: 2914: 2904: 2872: 2863: 2862: 2860: 2858: 2843: 2837: 2836: 2826: 2816: 2783: 2777: 2776: 2765: 2759: 2758: 2747: 2741: 2731: 2720: 2710: 2687:Current Research 2669:Umbilical hernia 2652:craniosynostosis 2614:Common Mutations 2540: 2516: 2493: 2464: 2434: 2404: 2391:Two Hybrid Assay 2375: 2346: 2290: 2085:Internal Repeats 2010: 1811: 1802: 1147:Pygmy Chimpanzee 1121:Accession Number 1107: 1035: 1034: 1006: 999: 982: 970: 961: 945: 941:RefSeq (protein) 931: 919: 910: 890: 866: 847: 821: 802: 776: 757: 726: 536: 522: 513: 506: 491: 431: 429:Top expressed in 424: 369: 367:Top expressed in 362: 341: 324: 314: 301: 290: 275: 268: 262: 251: 239: 223: 213: 200: 189: 174: 167: 161: 150: 136: 120: 114: 65: 58: 44: 32: 21: 4254: 4253: 4249: 4248: 4247: 4245: 4244: 4243: 4224: 4223: 4222: 4168: 4124: 4081: 4052: 4007: 3970: 3966: 3964:Further reading 3961: 3930: 3929: 3918: 3888: 3887: 3878: 3833: 3832: 3823: 3776: 3775: 3771: 3727: 3726: 3722: 3677: 3676: 3672: 3628: 3627: 3623: 3577: 3576: 3569: 3525: 3524: 3520: 3510: 3508: 3499: 3498: 3494: 3450: 3449: 3445: 3421:10.1.1.165.2784 3405: 3404: 3400: 3358: 3357: 3353: 3323: 3322: 3318: 3288: 3287: 3283: 3273: 3272: 3268: 3224: 3223: 3219: 3175: 3174: 3170: 3140: 3139: 3135: 3113: 3112: 3108: 3063: 3062: 3058: 3048: 3046: 3004: 3003: 2999: 2989: 2987: 2981: 2980: 2976: 2966: 2964: 2954: 2953: 2949: 2939: 2937: 2933: 2932: 2928: 2887:(11): 5857–64. 2874: 2873: 2866: 2856: 2854: 2851:MEGF8 Gene Card 2845: 2844: 2840: 2785: 2784: 2780: 2767: 2766: 2762: 2749: 2748: 2744: 2732: 2723: 2711: 2702: 2698: 2689: 2684: 2642: 2630: 2621: 2616: 2572: 2570:Splice Variants 2567: 2553:Uncharacterized 2538: 2530:Uncharacterized 2514: 2506:Uncharacterized 2491: 2470:High Everywhere 2462: 2432: 2402: 2397:IntAct, STRING 2373: 2344: 2288: 2277: 2272: 2220: 2212: 2207: 2187: 2178:Phobius, SMART 2071:Phosphorylation 2060:3 (confidently) 2003: 1978: 1925:EGF_Like Domain 1823:Number in MEGF8 1803: 1796: 1767:EGF-like domain 1748:EGF-like domain 1741:EGF-like domain 1724: 1712: 1699:disulfide bonds 1694: 1689: 1684: 1619: 1606:Wayback Machine 1595: 1586: 1451:Oryzias latipes 1433:Channel Catfish 1389:African Cichlid 1213:Florida Manatee 1096: 1091: 1044:View/Edit Mouse 1039:View/Edit Human 1002: 995: 992:Location (UCSC) 978: 957: 953: 927: 906: 902: 898: 811:ENSG00000105429 704: 593: 562: 558:protein binding 518: 487: 478: 473: 469: 465: 461: 457: 455:ascending aorta 453: 449: 445: 441: 427: 416: 411: 407: 403: 399: 395: 391: 387: 383: 379: 365: 309: 296: 288: 278: 277: 276: 269: 249: 226:Gene location ( 208: 195: 187: 177: 176: 175: 168: 146: 123:Gene location ( 74: 61: 54: 28: 23: 22: 15: 12: 11: 5: 4252: 4250: 4242: 4241: 4239:Kelch proteins 4236: 4226: 4225: 4221: 4220: 4182:(9): 3219–24. 4166: 4138:(5): 897–905. 4122: 4079: 4050: 4005: 3967: 3965: 3962: 3960: 3959: 3916: 3876: 3847:(5): 897–905. 3821: 3769: 3720: 3670: 3621: 3584:Genome Biology 3567: 3518: 3492: 3443: 3398: 3371:(6): 1633–49. 3351: 3316: 3297:(5): 1351–62. 3281: 3266: 3217: 3168: 3133: 3106: 3056: 3020:(3): 363–371. 2997: 2982:Pappas Jr GJ. 2974: 2947: 2926: 2864: 2838: 2799:(9): 3219–24. 2778: 2760: 2742: 2721: 2699: 2697: 2694: 2688: 2685: 2683: 2682: 2681:("knock-knee") 2676: 2673:Cryptorchidism 2670: 2667: 2664: 2661: 2658: 2655: 2647: 2641: 2638: 2629: 2626: 2620: 2617: 2615: 2612: 2571: 2568: 2566: 2563: 2560: 2559: 2557: 2554: 2551: 2548: 2546: 2544: 2541: 2535: 2534: 2531: 2528: 2525: 2522: 2520: 2517: 2511: 2510: 2507: 2504: 2501: 2499: 2497: 2494: 2488: 2487: 2484: 2481: 2478: 2471: 2468: 2465: 2459: 2458: 2455: 2451: 2448: 2441: 2438: 2435: 2429: 2428: 2425: 2421: 2418: 2411: 2408: 2405: 2399: 2398: 2395: 2392: 2389: 2382: 2379: 2376: 2370: 2369: 2366: 2362: 2359: 2353: 2350: 2347: 2341: 2340: 2333: 2326: 2319: 2312: 2305: 2298: 2284: 2276: 2273: 2271: 2270: 2267: 2264: 2261: 2258: 2255: 2252: 2249: 2246: 2243: 2240: 2237: 2234: 2231: 2228: 2224: 2219: 2216: 2211: 2208: 2206: 2203: 2186: 2183: 2180: 2179: 2176: 2173: 2170: 2166: 2165: 2162: 2159: 2156: 2152: 2151: 2148: 2145: 2142: 2138: 2137: 2134: 2131: 2128: 2124: 2123: 2120: 2117: 2114: 2110: 2109: 2106: 2103: 2100: 2096: 2095: 2092: 2089: 2086: 2082: 2081: 2078: 2075: 2072: 2068: 2067: 2064: 2061: 2058: 2054: 2053: 2050: 2047: 2044: 2040: 2039: 2032: 2025: 2018: 2002: 1999: 1982:beta propeller 1977: 1974: 1955: 1954: 1951: 1948: 1944: 1943: 1940: 1937: 1936:EGF_LAM Domain 1933: 1932: 1929: 1926: 1922: 1921: 1918: 1915: 1911: 1910: 1907: 1904: 1900: 1899: 1896: 1893: 1889: 1888: 1885: 1882: 1878: 1877: 1874: 1871: 1867: 1866: 1863: 1860: 1856: 1855: 1852: 1849: 1845: 1844: 1841: 1838: 1837:Signal Peptide 1834: 1833: 1826: 1819: 1795: 1792: 1791: 1790: 1770: 1763: 1760:Leucine Zipper 1757: 1751: 1744: 1738: 1735: 1723: 1720: 1711: 1708: 1693: 1690: 1688: 1685: 1683: 1682: 1679: 1676: 1673: 1670: 1667: 1664: 1661: 1658: 1655: 1652: 1649: 1646: 1643: 1640: 1637: 1634: 1631: 1627: 1618: 1615: 1594: 1591: 1585: 1582: 1579: 1578: 1575: 1572: 1569: 1566: 1563: 1557: 1556: 1553: 1550: 1547: 1544: 1541: 1535: 1534: 1531: 1528: 1525: 1522: 1519: 1513: 1512: 1509: 1506: 1503: 1500: 1497: 1491: 1490: 1487: 1484: 1481: 1478: 1475: 1473:Apis mellifera 1469: 1468: 1465: 1462: 1459: 1456: 1453: 1447: 1446: 1443: 1440: 1437: 1434: 1431: 1425: 1424: 1421: 1418: 1415: 1412: 1409: 1403: 1402: 1399: 1396: 1393: 1390: 1387: 1381: 1380: 1377: 1374: 1371: 1368: 1365: 1359: 1358: 1355: 1352: 1349: 1346: 1343: 1337: 1336: 1333: 1330: 1327: 1324: 1321: 1315: 1314: 1311: 1308: 1305: 1302: 1299: 1293: 1292: 1289: 1286: 1283: 1282:NP_001153872.1 1280: 1277: 1271: 1270: 1267: 1264: 1261: 1258: 1255: 1249: 1248: 1245: 1242: 1239: 1236: 1233: 1227: 1226: 1223: 1220: 1217: 1214: 1211: 1205: 1204: 1201: 1198: 1195: 1192: 1189: 1183: 1182: 1179: 1176: 1173: 1170: 1167: 1161: 1160: 1157: 1154: 1151: 1148: 1145: 1139: 1138: 1133: 1128: 1123: 1118: 1113: 1095: 1092: 1090: 1087: 1058:also known as 1051: 1050: 1047: 1046: 1041: 1031: 1030: 1024: 1023: 1020: 1019: 1017: 1015: 1008: 1007: 1000: 993: 989: 988: 985: 984: 974: 973: 967: 964: 963: 949: 948: 942: 938: 937: 934: 933: 923: 922: 916: 913: 912: 894: 893: 887: 883: 882: 879: 878: 870: 869: 863: 860: 859: 851: 850: 844: 838: 837: 834: 833: 825: 824: 818: 815: 814: 806: 805: 799: 793: 792: 789: 788: 780: 779: 773: 770: 769: 761: 760: 754: 748: 747: 742: 737: 733: 732: 722: 721: 718: 717: 706: 705: 703: 702: 697: 692: 687: 682: 677: 672: 667: 662: 657: 652: 647: 642: 637: 632: 627: 622: 617: 612: 607: 601: 599: 595: 594: 592: 591: 586: 581: 576: 570: 568: 564: 563: 561: 560: 555: 549: 547: 543: 542: 532: 531: 528: 527: 524: 523: 515: 514: 503: 497: 496: 493: 492: 484: 483: 480: 479: 477: 476: 472: 468: 464: 460: 456: 452: 448: 444: 440: 436: 433: 432: 421: 418: 417: 415: 414: 410: 406: 402: 398: 394: 390: 386: 382: 378: 374: 371: 370: 358: 357: 349: 338: 332: 331: 328:RNA expression 320: 319: 316: 315: 307: 303: 302: 294: 291: 286: 280: 279: 270: 263: 257: 253: 252: 247: 241: 240: 232: 231: 219: 218: 215: 214: 206: 202: 201: 193: 190: 185: 179: 178: 169: 162: 156: 152: 151: 144: 138: 137: 129: 128: 116: 115: 72: 68: 67: 59: 51: 50: 46: 45: 37: 36: 26: 24: 14: 13: 10: 9: 6: 4: 3: 2: 4251: 4240: 4237: 4235: 4232: 4231: 4229: 4217: 4213: 4208: 4203: 4198: 4193: 4189: 4185: 4181: 4177: 4173: 4167: 4163: 4159: 4154: 4149: 4145: 4141: 4137: 4133: 4129: 4123: 4119: 4115: 4110: 4105: 4101: 4097: 4093: 4089: 4085: 4080: 4076: 4072: 4068: 4064: 4060: 4056: 4051: 4047: 4043: 4038: 4033: 4028: 4023: 4019: 4015: 4011: 4006: 4002: 3998: 3994: 3990: 3986: 3982: 3978: 3974: 3969: 3968: 3963: 3955: 3951: 3947: 3943: 3940:(2): 311–24. 3939: 3935: 3927: 3925: 3923: 3921: 3917: 3912: 3908: 3904: 3900: 3896: 3892: 3885: 3883: 3881: 3877: 3872: 3868: 3863: 3858: 3854: 3850: 3846: 3842: 3838: 3830: 3828: 3826: 3822: 3817: 3813: 3808: 3803: 3799: 3795: 3791: 3787: 3783: 3779: 3773: 3770: 3765: 3761: 3756: 3751: 3747: 3743: 3739: 3735: 3731: 3724: 3721: 3716: 3712: 3707: 3702: 3698: 3694: 3690: 3686: 3682: 3674: 3671: 3666: 3662: 3657: 3652: 3648: 3644: 3640: 3636: 3632: 3625: 3622: 3617: 3613: 3608: 3603: 3598: 3593: 3589: 3585: 3581: 3574: 3572: 3568: 3563: 3559: 3554: 3549: 3545: 3541: 3537: 3533: 3529: 3522: 3519: 3506: 3502: 3496: 3493: 3488: 3484: 3479: 3474: 3470: 3466: 3462: 3458: 3454: 3447: 3444: 3439: 3435: 3431: 3427: 3422: 3417: 3414:(4): 783–95. 3413: 3409: 3402: 3399: 3394: 3390: 3386: 3382: 3378: 3374: 3370: 3366: 3362: 3355: 3352: 3347: 3343: 3339: 3335: 3332:(3): 360–71. 3331: 3327: 3320: 3317: 3312: 3308: 3304: 3300: 3296: 3292: 3285: 3282: 3277: 3276:Science Press 3270: 3267: 3262: 3258: 3253: 3248: 3244: 3240: 3236: 3232: 3228: 3221: 3218: 3213: 3209: 3204: 3199: 3195: 3191: 3187: 3183: 3179: 3172: 3169: 3164: 3160: 3156: 3152: 3148: 3144: 3137: 3134: 3129: 3125: 3121: 3117: 3110: 3107: 3102: 3098: 3093: 3088: 3084: 3080: 3076: 3072: 3068: 3060: 3057: 3045: 3041: 3036: 3035:10044/1/18157 3031: 3027: 3023: 3019: 3015: 3011: 3007: 3001: 2998: 2985: 2978: 2975: 2962: 2958: 2951: 2948: 2936: 2930: 2927: 2922: 2918: 2913: 2908: 2903: 2898: 2894: 2890: 2886: 2882: 2878: 2871: 2869: 2865: 2852: 2848: 2842: 2839: 2834: 2830: 2825: 2820: 2815: 2810: 2806: 2802: 2798: 2794: 2790: 2782: 2779: 2774: 2770: 2764: 2761: 2756: 2752: 2746: 2743: 2739: 2735: 2730: 2728: 2726: 2722: 2718: 2714: 2709: 2707: 2705: 2701: 2695: 2693: 2686: 2680: 2677: 2674: 2671: 2668: 2665: 2662: 2659: 2656: 2653: 2649: 2648: 2646: 2639: 2637: 2635: 2627: 2625: 2618: 2613: 2607: 2603: 2600: 2596: 2593: 2589: 2586: 2582: 2579: 2575: 2569: 2564: 2558: 2555: 2552: 2549: 2547: 2545: 2542: 2537: 2536: 2532: 2529: 2526: 2523: 2521: 2518: 2513: 2512: 2508: 2505: 2502: 2500: 2498: 2495: 2490: 2489: 2485: 2482: 2479: 2476: 2472: 2469: 2466: 2461: 2460: 2456: 2452: 2449: 2446: 2442: 2439: 2436: 2431: 2430: 2426: 2424:stabilization 2422: 2419: 2416: 2412: 2409: 2406: 2401: 2400: 2396: 2393: 2390: 2387: 2383: 2380: 2377: 2372: 2371: 2367: 2363: 2360: 2357: 2354: 2351: 2348: 2343: 2342: 2339: 2338: 2334: 2332: 2331: 2327: 2325: 2324: 2320: 2318: 2317: 2313: 2311: 2310: 2306: 2304: 2303: 2299: 2297: 2296: 2292: 2291: 2287: 2281: 2274: 2268: 2265: 2262: 2259: 2256: 2253: 2250: 2247: 2244: 2241: 2238: 2235: 2232: 2229: 2226: 2225: 2223: 2217: 2215: 2209: 2204: 2198: 2194: 2192: 2184: 2177: 2174: 2171: 2168: 2167: 2163: 2160: 2157: 2154: 2153: 2149: 2146: 2143: 2140: 2139: 2135: 2132: 2129: 2126: 2125: 2121: 2118: 2115: 2112: 2111: 2107: 2104: 2101: 2098: 2097: 2093: 2090: 2087: 2084: 2083: 2079: 2076: 2073: 2070: 2069: 2065: 2062: 2059: 2056: 2055: 2051: 2048: 2045: 2042: 2041: 2038: 2037: 2033: 2031: 2030: 2026: 2024: 2023: 2019: 2017: 2016: 2012: 2011: 2008: 2000: 1998: 1995: 1991: 1987: 1983: 1975: 1969: 1961: 1952: 1949: 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950: 946: 943: 939: 932: 930: 924: 920: 917: 911: 909: 905: 901: 895: 891: 888: 886:RefSeq (mRNA) 884: 877: 876: 871: 867: 864: 858: 857: 852: 848: 845: 843: 839: 832: 831: 826: 822: 819: 813: 812: 807: 803: 800: 798: 794: 787: 786: 781: 777: 774: 768: 767: 762: 758: 755: 753: 749: 746: 743: 741: 738: 734: 731: 727: 723: 716: 712: 707: 701: 698: 696: 693: 691: 688: 686: 683: 681: 678: 676: 673: 671: 668: 666: 663: 661: 658: 656: 653: 651: 648: 646: 643: 641: 638: 636: 633: 631: 628: 626: 623: 621: 618: 616: 613: 611: 608: 606: 603: 602: 600: 597: 596: 590: 587: 585: 582: 580: 577: 575: 572: 571: 569: 566: 565: 559: 556: 554: 551: 550: 548: 545: 544: 541: 540:Gene ontology 537: 533: 521: 516: 512: 507: 504: 502: 498: 490: 485: 474: 470: 466: 462: 458: 454: 450: 446: 442: 439:otolith organ 438: 437: 434: 430: 425: 422: 413:parotid gland 412: 408: 404: 400: 396: 392: 388: 384: 380: 376: 375: 372: 368: 363: 360: 359: 356: 354: 350: 348: 347: 343: 342: 339: 337: 333: 329: 325: 321: 313: 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Retrieved 3504: 3495: 3460: 3456: 3446: 3411: 3407: 3401: 3368: 3364: 3354: 3329: 3325: 3319: 3294: 3290: 3284: 3275: 3269: 3234: 3230: 3220: 3185: 3181: 3171: 3146: 3142: 3136: 3122:(5): 410–9. 3119: 3115: 3109: 3074: 3070: 3059: 3047:. Retrieved 3017: 3013: 3000: 2988:. Retrieved 2977: 2965:. Retrieved 2960: 2950: 2938:. Retrieved 2929: 2884: 2880: 2855:. Retrieved 2850: 2841: 2796: 2792: 2781: 2772: 2763: 2754: 2745: 2690: 2643: 2631: 2622: 2598: 2597: 2591: 2590: 2584: 2583: 2577: 2576: 2573: 2384:Atrophin 1 ( 2336: 2335: 2329: 2328: 2322: 2321: 2315: 2314: 2308: 2307: 2301: 2300: 2294: 2293: 2285: 2278: 2221: 2213: 2188: 2035: 2034: 2028: 2027: 2021: 2020: 2014: 2013: 2006: 1979: 1881:Kelch Repeat 1829: 1828: 1822: 1821: 1815: 1814: 1799: 1725: 1713: 1695: 1622: 1620: 1609: 1596: 1587: 1568:XP_001635521 1480:XP_006568067 1458:XP_004078282 1414:XP_005158088 1392:XP_006808273 1370:XP_002936442 1348:XP_006038171 1326:XP_006273703 1275:Mus musculus 1238:XP_006748348 1235:Weddell Seal 1216:XP_004388865 1194:XP_004271289 1172:XP_005909034 1150:XP_003811808 1143:Pan Paniscus 1136:Length (AAs) 1135: 1130: 1125: 1120: 1115: 1110: 1103: 1097: 1059: 1055: 1054: 980:NP_001153872 977: 955:NP_001258867 952: 929:NM_001160400 926: 904:NM_001271938 897: 873: 854: 828: 809: 783: 764: 744: 739: 447:otic vesicle 393:frontal pole 351: 344: 71:External IDs 29: 3505:GeoProfiles 3149:(1): 34–6. 2955:Brendel V. 2679:Genu valgum 2543:Conf: 0.370 2519:Conf: 0.370 2496:Conf: 0.370 2467:Conf: 0.778 2437:Conf: 0.510 2407:Conf: 0.510 2378:Conf: 0.538 2316:Description 2057:SUMOylation 1986:kelch motif 1778:semaphorins 1754:Kelch motif 1407:Danio rerio 1260:NP_446080.1 1085:subtype 2. 310:25,065,342 297:25,016,589 289:7|7 A3 209:42,378,769 196:42,325,609 49:Identifiers 4228:Categories 4094:: 127–34. 4020:: e01160. 3365:Proteomics 2857:4 February 2740:, May 2017 2719:, May 2017 2696:References 2381:Everywhere 2349:Conf:0.866 2302:Confidence 2185:Expression 1953:2588-2610 1942:1151-1199 1920:1014-1055 1903:PSI Domain 1898:1698-1719 1848:CUB Domain 1732:CUB domain 1411:Zebra fish 1301:King Cobra 1191:Orca Whale 355:(ortholog) 92:HomoloGene 3778:Maglott D 3416:CiteSeerX 3278:(4): 181. 3006:Kelley LA 2365:pathways. 2175:2611-2785 2161:2588-2610 2133:2588-2610 2108:NetNGlyc 2066:SUMOplot 1782:integrins 1593:Promoters 1546:XP_789561 1165:Bos Mutus 959:NP_001401 908:NM_001410 900:NM_178121 730:Orthologs 100:GeneCards 4216:19218456 4162:23063620 4118:24713578 4055:Genomics 4046:24052814 3993:24458945 3871:23063620 3816:21115458 3764:18940858 3715:22121220 3665:22139911 3616:19919682 3562:21097893 3511:15 April 3487:17483518 3438:15223320 3393:18810164 3385:15174133 3311:10600390 3261:16844986 3212:18000004 3163:10087920 3101:21109532 3049:27 April 3044:19247286 2990:24 April 2967:27 April 2833:19218456 2736:– 2715:– 2675:in males 2463:SMARCD3 2330:Function 2309:Location 2150:Phobius 2122:SignalP 2080:NetPhos 2015:Feature 1765:Laminin 1746:Calcium 1602:Archived 1584:Paralogs 1524:EFX84934 1502:JAB95791 1436:AHI50432 1304:ETE71721 1028:Wikidata 709:Sources: 579:membrane 4207:2651267 4184:Bibcode 4153:3487118 4109:4122622 4075:9693030 4037:3776557 4001:3040251 3954:3322002 3862:3487118 3807:3013746 3755:2686466 3706:3245075 3656:3245017 3607:3091323 3553:3013736 3478:1933244 3346:7583634 3252:1538823 3203:2238974 3128:2288911 3092:3013737 2940:8 March 2935:"BLAST" 2921:9600884 2889:Bibcode 2824:2651267 2801:Bibcode 2738:Ensembl 2717:Ensembl 2486:STRING 2475:SMARCD3 2433:CACNA1A 2147:1- 2587 1854:40-147 1774:plexins 842:UniProt 797:Ensembl 736:Species 715:QuickGO 589:nucleus 443:utricle 330:pattern 188:19q13.2 88:2446294 56:Aliases 4214:  4204:  4160:  4150:  4116:  4106:  4073:  4044:  4034:  3999:  3991:  3952:  3911:263437 3909:  3869:  3859:  3814:  3804:  3762:  3752:  3713:  3703:  3663:  3653:  3614:  3604:  3560:  3550:  3507:. NCBI 3485:  3475:  3436:  3418:  3391:  3383:  3344:  3309:  3259:  3249:  3210:  3200:  3161:  3126:  3099:  3089:  3042:  2919:  2909:  2831:  2821:  2632:Visit 2454:death. 2445:Cav2.1 2337:Source 2036:Source 1789:cells. 1786:Plexin 1717:PHYRE2 1610:megf8. 1014:search 1012:PubMed 875:P60882 856:Q7Z7M0 785:269878 752:Entrez 501:BioGPS 80:604267 4014:eLife 3997:S2CID 3389:S2CID 2912:34487 2515:Y3542 2492:FIHB1 2415:ATXN7 2403:ATXN7 2356:GFI1B 2345:GFI1B 2136:SAPS 2094:SAPS 1843:1-34 1623:megf8 1577:2534 1533:2888 1511:2959 1489:2913 1467:2952 1445:2875 1423:2870 1401:2813 1379:2730 1357:2465 1335:2793 1291:2789 1279:Mouse 1269:2789 1247:2068 1225:2708 1203:2789 1181:2842 1159:2778 1069:BLAST 1056:Megf8 745:Mouse 740:Human 711:Amigo 353:Mouse 346:Human 293:Start 228:Mouse 192:Start 125:Human 104:MEGF8 96:15988 63:MEGF8 35:MEGF8 18:MEGF8 4212:PMID 4158:PMID 4114:PMID 4071:PMID 4042:PMID 3989:PMID 3977:164A 3950:PMID 3907:PMID 3867:PMID 3812:PMID 3760:PMID 3711:PMID 3661:PMID 3612:PMID 3558:PMID 3513:2014 3483:PMID 3434:PMID 3381:PMID 3342:PMID 3307:PMID 3257:PMID 3208:PMID 3159:PMID 3124:PMID 3097:PMID 3051:2014 3040:PMID 2992:2014 2969:2014 2961:SAPS 2942:2014 2917:PMID 2859:2014 2829:PMID 2619:SNPs 2539:ProW 2386:ATN1 2374:ATN1 2191:NCBI 1990:SCOP 1780:and 1555:194 1313:404 1089:Gene 766:1954 336:Bgee 284:Band 245:Chr. 183:Band 142:Chr. 76:OMIM 4202:PMC 4192:doi 4180:106 4148:PMC 4140:doi 4104:PMC 4096:doi 4063:doi 4032:PMC 4022:doi 3981:doi 3942:doi 3899:doi 3857:PMC 3849:doi 3802:PMC 3794:doi 3750:PMC 3742:doi 3701:PMC 3693:doi 3651:PMC 3643:doi 3602:PMC 3592:doi 3548:PMC 3540:doi 3473:PMC 3465:doi 3426:doi 3412:340 3373:doi 3334:doi 3299:doi 3295:294 3247:PMC 3239:doi 3198:PMC 3190:doi 3151:doi 3087:PMC 3079:doi 3030:hdl 3022:doi 2907:PMC 2897:doi 2819:PMC 2809:doi 2797:106 2074:116 1574:51% 1571:38% 1552:51% 1549:37% 1530:48% 1527:35% 1508:45% 1505:32% 1486:45% 1483:31% 1464:67% 1461:54% 1442:77% 1439:54% 1420:66% 1417:54% 1398:67% 1395:55% 1376:67% 1373:56% 1354:75% 1351:67% 1332:71% 1329:63% 1310:70% 1307:63% 1288:90% 1285:89% 1266:89% 1263:88% 1257:Rat 1244:92% 1241:91% 1222:89% 1219:88% 1200:94% 1197:93% 1178:82% 1175:79% 1169:Yak 1156:99% 1153:99% 306:End 205:End 108:OMA 84:MGI 4230:: 4210:. 4200:. 4190:. 4178:. 4174:. 4156:. 4146:. 4136:91 4134:. 4130:. 4112:. 4102:. 4092:27 4090:. 4086:. 4069:. 4059:51 4057:. 4040:. 4030:. 4016:. 4012:. 3995:. 3987:. 3975:. 3948:. 3938:28 3936:. 3919:^ 3905:. 3893:. 3879:^ 3865:. 3855:. 3845:91 3843:. 3839:. 3824:^ 3810:. 3800:. 3790:39 3788:. 3784:. 3758:. 3748:. 3738:37 3736:. 3732:. 3709:. 3699:. 3689:40 3687:. 3683:. 3659:. 3649:. 3639:40 3637:. 3633:. 3610:. 3600:. 3588:10 3586:. 3582:. 3570:^ 3556:. 3546:. 3536:39 3534:. 3530:. 3503:. 3481:. 3471:. 3461:35 3459:. 3455:. 3432:. 3424:. 3410:. 3387:. 3379:. 3367:. 3363:. 3340:. 3328:. 3305:. 3293:. 3255:. 3245:. 3235:34 3233:. 3229:. 3206:. 3196:. 3186:36 3184:. 3180:. 3157:. 3147:24 3145:. 3118:. 3095:. 3085:. 3075:39 3073:. 3069:. 3038:. 3028:. 3016:. 3012:. 2959:. 2915:. 2905:. 2895:. 2885:95 2883:. 2879:. 2867:^ 2849:. 2827:. 2817:. 2807:. 2795:. 2791:. 2771:. 2753:. 2724:^ 2703:^ 2599:D: 2592:C: 2585:B: 2578:A: 2102:20 1784:. 1776:, 713:/ 312:bp 299:bp 211:bp 198:bp 106:; 102:: 98:; 94:: 90:; 86:: 82:; 78:: 4218:. 4194:: 4186:: 4164:. 4142:: 4120:. 4098:: 4077:. 4065:: 4048:. 4024:: 4018:2 4003:. 3983:: 3956:. 3944:: 3913:. 3901:: 3895:2 3873:. 3851:: 3818:. 3796:: 3766:. 3744:: 3717:. 3695:: 3667:. 3645:: 3618:. 3594:: 3564:. 3542:: 3515:. 3489:. 3467:: 3440:. 3428:: 3395:. 3375:: 3369:4 3348:. 3336:: 3330:5 3313:. 3301:: 3263:. 3241:: 3214:. 3192:: 3165:. 3153:: 3130:. 3120:2 3103:. 3081:: 3053:. 3032:: 3024:: 3018:4 2994:. 2971:. 2944:. 2923:. 2899:: 2891:: 2861:. 2835:. 2811:: 2803:: 2775:. 2757:. 2654:) 2477:) 2447:) 2417:) 2388:) 2172:1 2158:1 2144:1 2130:1 2116:1 2088:1 2077:- 2049:- 1950:1 1939:1 1928:4 1917:1 1906:6 1895:1 1884:9 1873:2 1862:6 1851:1 1840:1 230:) 127:) 110:: 20:)

Index

MEGF8

Aliases
MEGF8
OMIM
604267
MGI
2446294
HomoloGene
15988
GeneCards
MEGF8
OMA
MEGF8 - orthologs
Human
Chromosome 19 (human)
Chr.
Chromosome 19 (human)
Chromosome 19 (human)
Genomic location for MEGF8
Genomic location for MEGF8
Band
bp
bp
Mouse
Chromosome 7 (mouse)
Chr.
Chromosome 7 (mouse)
Genomic location for MEGF8
Genomic location for MEGF8

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