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FANCE

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309: 286: 183: 208: 2818: 560: 1052:. Fanconi anemia is a genetically heterogeneous recessive disorder characterized by cytogenetic instability, hypersensitivity to DNA cross-linking agents, increased chromosomal breakage, and defective DNA repair. The members of the Fanconi anemia complementation group do not share sequence similarity; they are related by their assembly into a common nuclear protein complex. This gene encodes the protein for complementation groufcrp E. 315: 214: 36: 1207:, where it is fused with 3 DNA cells that will help in calculating the sensitivity to composites of Mitomycin C, a DNA cross-linking agent (Sigma). It also then examines the use of micro satellite markers D6S422 and D6S1610, for linking. From this, a chromosomal region on chromosome 6p is located for FANCE. 62: 1870:
de Winter JP, Léveillé F, van Berkel CG, Rooimans MA, van Der Weel L, Steltenpool J, Demuth I, Morgan NV, Alon N, Bosnoyan-Collins L, Lightfoot J, Leegwater PA, Waisfisz Q, Komatsu K, Arwert F, Pronk JC, Mathew CG, Digweed M, Buchwald M, Joenje H (November 2000).
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de Winter JP, Léveillé F, van Berkel CG, Rooimans MA, van Der Weel L, Steltenpool J, Demuth I, Morgan NV, Alon N, Bosnoyan-Collins L, Lightfoot J, Leegwater PA, Waisfisz Q, Komatsu K, Arwert F, Pronk JC, Mathew CG, Digweed M, Buchwald M, Joenje H (November 2000).
1156:-helix and no β-strand. Long shaped, non-globular shape and 70 Å n size. Width of 30 Å and thickness 20 Å. The protein folds continuously in right-handed manner from N- to C- terminal. Identifying it is easy because of its helices at the end of C-end. 1213:
showed that FANCE-L348M and FANCE-E263K mutants showed a division in the nuclear membrane of FA-E EUFA409 LCL indicating that irrespective of FANCE having putative nuclear localization signals, it limits primarily to the
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Meetei AR, de Winter JP, Medhurst AL, Wallisch M, Waisfisz Q, van de Vrugt HJ, Oostra AB, Yan Z, Ling C, Bishop CE, Hoatlin ME, Joenje H, Wang W (October 2003). "A novel ubiquitin ligase is deficient in Fanconi anemia".
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Meetei AR, de Winter JP, Medhurst AL, Wallisch M, Waisfisz Q, van de Vrugt HJ, Oostra AB, Yan Z, Ling C, Bishop CE, Hoatlin ME, Joenje H, Wang W (October 2003). "A novel ubiquitin ligase is deficient in Fanconi anemia".
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The main complex of FA contains a nuclear multi-subunit complex of notably 8 FA proteins. This adds a single ubiquitin chain to the FANCD2 following DNA damage or duplicative pressure.
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Léveillé F, Blom E, Medhurst AL, Bier P, Laghmani M, Johnson M, Rooimans MA, Sobeck A, Waisfisz Q, Arwert F, Patel KJ, Hoatlin ME, Joenje H, de Winter JP (September 2004).
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Waisfisz Q, Saar K, Morgan NV, Altay C, Leegwater PA, de Winter JP, Komatsu K, Evans GR, Wegner RD, Reis A, Joenje H, Arwert F, Mathew CG, Pronk JC, Digweed M (May 1999).
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Waisfisz Q, Saar K, Morgan NV, Altay C, Leegwater PA, de Winter JP, Komatsu K, Evans GR, Wegner RD, Reis A, Joenje H, Arwert F, Mathew CG, Pronk JC, Digweed M (May 1999).
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FANCD2, BRCA2 and constructed nuclear foci. Also, as it is the only member showing direct union with FANCD2 and gives the needed links between FA core complex and FANCD2.
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on its surface that is found to be important for its binding with FANCD2. The existence of recurrent helical motif was not clear when analysis of amino acids was done.
1196:(Immunohistochemistry) where the predicted molecular weight was 58 kDa in Western blot and antigen recovery with citrate buffer pH6 was done before the onset of IHC-P. 1133:
For the collection of FANCC, FANCE is important in the nucleus and gathering of the core complex. Some characteristics of FANCE are that it can set itself up with
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Wegner RD, Henrichs I, Joenje H, Schroeder-Kurth T (December 1996). "Fanconi anemia complementation group E: clinical and cytogenetic data of the first patient".
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Meetei AR, Medhurst AL, Ling C, Xue Y, Singh TR, Bier P, Steltenpool J, Stone S, Dokal I, Mathew CG, Hoatlin M, Joenje H, de Winter JP, Wang W (September 2005).
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Hussain S, Wilson JB, Medhurst AL, Hejna J, Witt E, Ananth S, Davies A, Masson JY, Moses R, West SC, de Winter JP, Ashworth A, Jones NJ, Mathew CG (June 2004).
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Hussain S, Wilson JB, Medhurst AL, Hejna J, Witt E, Ananth S, Davies A, Masson JY, Moses R, West SC, de Winter JP, Ashworth A, Jones NJ, Mathew CG (June 2004).
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Yin, H.; Suye, S.; Zhou, Z.; Cai, H.; Fu, C. (2022). "The reduction of oocytes and disruption of the meiotic prophase I in Fanconi anemia E-deficient mice".
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Meetei AR, Levitus M, Xue Y, Medhurst AL, Zwaan M, Ling C, Rooimans MA, Bier P, Hoatlin M, Pals G, de Winter JP, Wang W, Joenje H (November 2004).
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Joenje H, Lo ten Foe JR, Oostra AB, van Berkel CG, Rooimans MA, Schroeder-Kurth T, Wegner RD, Gille JJ, Buchwald M, Arwert F (September 1995).
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The location at molecular level is in base pairs 35,452,339 to 35,467,106 on chromosome 6 (Homo sapiens Annotation Release 109, GRCh38.p12)
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Joenje H, Oostra AB, Wijker M, di Summa FM, van Berkel CG, Rooimans MA, Ebell W, van Weel M, Pronk JC, Buchwald M, Arwert F (October 1997).
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It restores DNA cross-links and is needed for nuclear accumulation of FANCC, delivering a critical bridge between FA complex and FANCD2.
308: 954: 947: 285: 1447: 1304: 1283: 2714:"FANCC, FANCE, and FANCD2 form a ternary complex essential to the integrity of the Fanconi anemia DNA damage response pathway" 1300: 207: 182: 1279: 124: 1224: 321: 220: 1505:
van Twest S, Murphy VJ, Hodson C, Tan W, Swuec P, O'Rourke JJ, Heierhorst J, Crismani W, Deans AJ (January 2017).
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Pace P, Johnson M, Tan WM, Mosedale G, Sng C, Hoatlin M, de Winter J, Joenje H, Gergely F, Patel KJ (July 2002).
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Pace P, Johnson M, Tan WM, Mosedale G, Sng C, Hoatlin M, de Winter J, Joenje H, Gergely F, Patel KJ (July 2002).
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isoform. In normal, non-mutant cells, FANCD2 is mono-ubiquinated in response to DNA damage. FANCE together with
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Garcia-Higuera I, Taniguchi T, Ganesan S, Meyn MS, Timmers C, Hejna J, Grompe M, D'Andrea AD (February 2001).
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Garcia-Higuera I, Taniguchi T, Ganesan S, Meyn MS, Timmers C, Hejna J, Grompe M, D'Andrea AD (February 2001).
1355:"Classification of Fanconi anemia patients by complementation analysis: evidence for a fifth genetic subtype" 59: 2671:"A human ortholog of archaeal DNA repair protein Hef is defective in Fanconi anemia complementation group M" 769: 1100: 2783: 1193: 1092: 196: 2329:"Direct interactions of the five known Fanconi anaemia proteins suggest a common functional pathway" 1616:"Direct interactions of the five known Fanconi anaemia proteins suggest a common functional pathway" 111: 2442:"Fanconi anemia protein complex: mapping protein interactions in the yeast 2- and 3-hybrid systems" 2075:"Fanconi anemia protein complex: mapping protein interactions in the yeast 2- and 3-hybrid systems" 1119:
The location of the gene is in 6p21.31, where p is the short arm of chromosome 6 at position 21.31
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FANCE is stated to have been expressed in 151 organs with the highest level in female gonads.
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acts as the substrate adapter for this reaction Activated FANCD2 protein co-localizes with
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Meetei AR, Sechi S, Wallisch M, Yang D, Young MK, Joenje H, Hoatlin ME, Wang W (May 2003).
559: 152: 1557:"FANCE - Fanconi anemia group E protein - Homo sapiens (Human) - FANCE gene & protein" 1141: 376: 2695: 2670: 2310: 2285: 2267: 2242: 2217: 1897: 1872: 1847: 1822: 1725: 1700: 1421: 1396: 35: 2617: 2592: 2501: 2476: 2388: 2363: 2003: 1978: 1888: 1673: 1656: 1482: 1465: 1412: 658: 653: 648: 632: 627: 622: 606: 601: 2840: 2764: 2608: 2492: 1804: 1751: 588: 2548: 2233: 2056: 136: 1210: 1200: 1189: 1056: 394: 173: 2593:"Functional interaction of monoubiquitinated FANCD2 and BRCA2/FANCD1 in chromatin" 1873:"Isolation of a cDNA representing the Fanconi anemia complementation group E gene" 1397:"Isolation of a cDNA representing the Fanconi anemia complementation group E gene" 1523: 1506: 160: 1507:"Mechanism of Ubiquitination and Deubiquitination in the Fanconi Anemia Pathway" 1340:
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
2458: 2441: 2423: 2407:"The Fanconi anemia protein, FANCE, promotes the nuclear accumulation of FANCC" 2406: 2091: 2074: 1945: 1929:"The Fanconi anemia protein, FANCE, promotes the nuclear accumulation of FANCC" 1928: 1584:"FANCE FA complementation group E [Homo sapiens (human)] - Gene - NCBI" 477: 115:, FACE, FAE, Fanconi anemia complementation group E, FA complementation group E 1099:
chromosomes. Activated FANCD2 protein may function prior to the initiation of
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Medhurst AL, Huber PA, Waisfisz Q, de Winter JP, Mathew CG (February 2001).
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Medhurst AL, Huber PA, Waisfisz Q, de Winter JP, Mathew CG (February 2001).
1134: 1076: 688: 537: 415: 360: 347: 259: 246: 148: 2739: 2730: 2713: 2704: 2661: 2626: 2583: 2540: 2510: 2477:"A multiprotein nuclear complex connects Fanconi anemia and Bloom syndrome" 2467: 2432: 2397: 2379: 2354: 2345: 2328: 2319: 2185: 2176: 2159: 2141: 2100: 2048: 2012: 1994: 1954: 1906: 1856: 1796: 1734: 1682: 1641: 1632: 1615: 1542: 1491: 1430: 2276: 2225: 1657:"Interaction of the Fanconi anemia proteins and BRCA1 in a common pathway" 1466:"Interaction of the Fanconi anemia proteins and BRCA1 in a common pathway" 1380: 994: 989: 2574: 2558:"Direct interaction of FANCD2 with BRCA2 in DNA damage response pathways" 2557: 2132: 2116:"Direct interaction of FANCD2 with BRCA2 in DNA damage response pathways" 2115: 1716: 1583: 1556: 1204: 1172: 978: 814: 1788: 2826:: Crystal structure of human Fanconi Anemia protein E C-terminal domain 2769: 2759: 2364:"FANCE: the link between Fanconi anaemia complex assembly and activity" 1979:"FANCE: the link between Fanconi anaemia complex assembly and activity" 1533: 1176: 1096: 1010: 800: 755: 1816: 1814: 81: 2160:"The Fanconi anemia gene product FANCF is a flexible adaptor protein" 1237: 1168: 1072: 1037: 1020:. The Fanconi anemia complementation group (FANC) currently includes 962: 710: 20: 2686: 2652: 2635: 2532: 2301: 2258: 2040: 1838: 1248: 1243: 1231: 1084: 1080: 1068: 1064: 1060: 1049: 1045: 1041: 1033: 1025: 1021: 1701:"Insights into Fanconi Anaemia from the structure of human FANCE" 673: 669: 2636:"X-linked inheritance of Fanconi anemia complementation group B" 1017: 128: 2779: 2286:"The Fanconi anemia group E gene, FANCE, maps to chromosome 6p" 1823:"The Fanconi anemia group E gene, FANCE, maps to chromosome 6p" 568: 2775: 2754:
Overview of all the structural information available in the
1448:"Entrez Gene: FANCE Fanconi anemia, complementation group E" 1179:
indicating that FANCE has an essential role in meiosis.
384: 549: 925: 904: 870: 849: 2243:"Evidence for at least eight Fanconi anemia genes" 1296: 1294: 1292: 1275: 1273: 1271: 1167:FANCE-deficient mice exhibit a reduced number of 331: 230: 2591:Wang X, Andreassen PR, D'Andrea AD (July 2004). 1459: 1457: 2153: 2151: 2068: 2066: 1972: 1970: 1968: 1966: 1964: 1922: 1920: 1918: 1916: 1609: 1607: 1605: 1603: 1007:Fanconi anemia, complementation group E protein 16:Protein-coding gene in the species Homo sapiens 2712:Gordon SM, Alon N, Buchwald M (October 2005). 1301:GRCm38: Ensembl release 89: ENSMUSG00000007570 2791: 1059:complex containing FANCE protein (as well as 8: 1699:Nookala RK, Hussain S, Pellegrini L (2007). 1372:10.1182/blood.V86.6.2156.bloodjournal8662156 1280:GRCh38: Ensembl release 89: ENSG00000112039 2798: 2784: 2776: 1087:(breast cancer susceptibility protein) at 684: 584: 372: 271: 168: 70: 2729: 2694: 2651: 2616: 2573: 2500: 2457: 2422: 2405:Taniguchi T, D'Andrea AD (October 2002). 2387: 2344: 2309: 2266: 2175: 2131: 2090: 2002: 1944: 1927:Taniguchi T, D'Andrea AD (October 2002). 1896: 1846: 1724: 1672: 1631: 1532: 1522: 1481: 1420: 1370: 1071:) is essential for the activation of the 2768:(Fanconi anemia group E protein) at the 1752:"Anti-FANCE antibody (ab126177) | Abcam" 1442: 1440: 654:cellular response to DNA damage stimulus 2813: 1267: 25: 1746: 1744: 1694: 1692: 1578: 1576: 336: 297: 292: 235: 194: 189: 7: 2718:The Journal of Biological Chemistry 2440:Gordon SM, Buchwald M (July 2003). 2164:The Journal of Biological Chemistry 2073:Gordon SM, Buchwald M (July 2003). 2290:American Journal of Human Genetics 2247:American Journal of Human Genetics 2218:10.1111/j.1399-0004.1996.tb02716.x 1877:American Journal of Human Genetics 1827:American Journal of Human Genetics 1401:American Journal of Human Genetics 922: 901: 867: 846: 824: 805: 779: 760: 734: 715: 554: 472: 410: 389: 14: 1013:that in humans is encoded by the 2816: 2609:10.1128/MCB.24.13.5850-5862.2004 2493:10.1128/MCB.23.10.3417-3426.2003 1152:It consists of 13 α-helices, 1 3 558: 320: 313: 307: 284: 219: 212: 206: 181: 34: 623:Fanconi anaemia nuclear complex 2597:Molecular and Cellular Biology 2481:Molecular and Cellular Biology 1140:The structure of FANCE has an 569:More reference expression data 538:More reference expression data 1: 1889:10.1016/s0002-9297(07)62959-0 1674:10.1016/S1097-2765(01)00173-3 1483:10.1016/s1097-2765(01)00173-3 1413:10.1016/S0002-9297(07)62959-0 1188:FANCE has its application in 649:interstrand cross-link repair 305: 204: 1524:10.1016/j.molcel.2016.11.005 2847:Genes on human chromosome 6 2863: 2459:10.1182/blood-2002-11-3517 2424:10.1182/blood-2002-03-0860 2092:10.1182/blood-2002-11-3517 1946:10.1182/blood-2002-03-0860 18: 2811: 1336:"Mouse PubMed Reference:" 1318:"Human PubMed Reference:" 993: 988: 984: 977: 961: 942: 929: 908: 897: 874: 853: 842: 831: 827: 812: 808: 799: 786: 782: 767: 763: 754: 741: 737: 722: 718: 709: 694: 687: 683: 667: 587: 583: 566: 557: 548: 535: 484: 475: 422: 413: 383: 375: 371: 354: 341: 304: 283: 274: 270: 253: 240: 203: 180: 171: 167: 122: 119: 109: 102: 97: 78: 73: 56: 51: 46: 42: 33: 28: 2562:Human Molecular Genetics 2333:Human Molecular Genetics 2120:Human Molecular Genetics 1620:Human Molecular Genetics 1223:FANCE has been shown to 955:Chr 17: 28.53 – 28.55 Mb 19:Not to be confused with 1126:Protein Characteristics 948:Chr 6: 35.45 – 35.47 Mb 2731:10.1074/jbc.M507758200 2177:10.1074/jbc.M407034200 1705:Nucleic Acids Research 1199:FANCE is also used in 1093:synaptonemal complexes 488:neural layer of retina 57:Human UniProt search: 1101:meiotic recombination 1091:-induced foci and in 1036:(also called BRCA2), 299:Chromosome 17 (mouse) 2380:10.1093/emboj/cdf355 2346:10.1093/hmg/10.4.423 1995:10.1093/emboj/cdf355 1633:10.1093/hmg/10.4.423 1588:www.ncbi.nlm.nih.gov 1205:homozygosity mapping 1115:Chromosomal Location 462:gastrocnemius muscle 197:Chromosome 6 (human) 74:List of PDB id codes 47:Available structures 1789:10.1530/REP-21-0421 2575:10.1093/hmg/ddh135 2133:10.1093/hmg/ddh135 1717:10.1093/nar/gkm033 1171:and disruption of 1089:ionizing radiation 1077:mono-ubiquitinated 789:ENSMUSG00000007570 642:Biological process 616:Cellular component 602:molecular function 595:Molecular function 426:buccal mucosa cell 2834: 2833: 2206:Clinical Genetics 1148:Protein Structure 1004: 1003: 1000: 999: 973: 972: 938: 937: 919: 918: 893: 892: 864: 863: 838: 837: 821: 820: 795: 794: 776: 775: 750: 749: 731: 730: 679: 678: 579: 578: 575: 574: 544: 543: 531: 530: 469: 468: 367: 366: 266: 265: 161:FANCE - orthologs 93: 92: 89: 88: 2854: 2820: 2800: 2793: 2786: 2777: 2743: 2733: 2724:(43): 36118–25. 2708: 2698: 2665: 2655: 2630: 2620: 2587: 2577: 2552: 2514: 2504: 2471: 2461: 2436: 2426: 2401: 2391: 2368:The EMBO Journal 2358: 2348: 2323: 2313: 2280: 2270: 2237: 2190: 2189: 2179: 2170:(38): 39421–30. 2155: 2146: 2145: 2135: 2111: 2105: 2104: 2094: 2070: 2061: 2060: 2023: 2017: 2016: 2006: 1983:The EMBO Journal 1974: 1959: 1958: 1948: 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1219–24. 2640:Nature Genetics 2633: 2603:(13): 5850–62. 2590: 2555: 2521:Nature Genetics 2517: 2487:(10): 3417–26. 2474: 2439: 2404: 2374:(13): 3414–23. 2361: 2326: 2283: 2240: 2203: 2199: 2197:Further reading 2194: 2193: 2157: 2156: 2149: 2113: 2112: 2108: 2072: 2071: 2064: 2029:Nature Genetics 2025: 2024: 2020: 1989:(13): 3414–23. 1976: 1975: 1962: 1926: 1925: 1914: 1869: 1868: 1864: 1820: 1819: 1812: 1774: 1773: 1769: 1760: 1758: 1750: 1749: 1742: 1698: 1697: 1690: 1654: 1653: 1649: 1613: 1612: 1601: 1592: 1590: 1582: 1581: 1574: 1565: 1563: 1561:www.uniprot.org 1555: 1554: 1550: 1504: 1503: 1499: 1463: 1462: 1455: 1446: 1445: 1438: 1393: 1392: 1388: 1352: 1351: 1347: 1334: 1333: 1329: 1316: 1315: 1311: 1299: 1290: 1278: 1269: 1264: 1221: 1185: 1162: 1155: 1150: 1128: 1117: 1109: 1107:Gene Expression 1075:protein to the 995:View/Edit Mouse 990:View/Edit Human 953: 946: 943:Location (UCSC) 931: 910: 884: 880: 876: 855: 770:ENSG00000112039 663: 637: 611: 607:protein binding 567: 536: 527: 522: 518: 514: 510: 506: 502: 498: 494: 490: 476: 465: 460: 456: 452: 450:skin of abdomen 448: 446:tibial arteries 444: 440: 436: 432: 428: 414: 358: 345: 338:17|17 A3.3 337: 327: 326: 325: 318: 298: 275:Gene location ( 257: 244: 236: 226: 225: 224: 217: 195: 172:Gene location ( 123: 110: 103: 80: 58: 24: 17: 12: 11: 5: 2860: 2858: 2850: 2849: 2839: 2838: 2832: 2831: 2829: 2828: 2822: 2815: 2812: 2809: 2808: 2805: 2803: 2802: 2795: 2788: 2780: 2774: 2773: 2750: 2749:External links 2747: 2745: 2744: 2709: 2687:10.1038/ng1626 2666: 2653:10.1038/ng1458 2631: 2588: 2568:(12): 1241–8. 2553: 2533:10.1038/ng1241 2515: 2472: 2437: 2417:(7): 2457–62. 2402: 2359: 2324: 2302:10.1086/302385 2281: 2259:10.1086/514881 2238: 2200: 2198: 2195: 2192: 2191: 2147: 2126:(12): 1241–8. 2106: 2062: 2041:10.1038/ng1241 2018: 1960: 1939:(7): 2457–62. 1912: 1862: 1839:10.1086/302385 1810: 1767: 1740: 1711:(5): 1638–48. 1688: 1661:Molecular Cell 1647: 1599: 1572: 1548: 1517:(2): 247–259. 1511:Molecular Cell 1497: 1470:Molecular Cell 1453: 1436: 1386: 1365:(6): 2156–60. 1345: 1327: 1309: 1288: 1266: 1265: 1263: 1260: 1259: 1258: 1252: 1246: 1241: 1235: 1220: 1217: 1216: 1215: 1211:Immunoblotting 1208: 1197: 1184: 1181: 1161: 1158: 1153: 1149: 1146: 1127: 1124: 1116: 1113: 1108: 1105: 1002: 1001: 998: 997: 992: 982: 981: 975: 974: 971: 970: 968: 966: 959: 958: 951: 944: 940: 939: 936: 935: 927: 926: 920: 917: 916: 906: 905: 899: 895: 894: 891: 890: 872: 871: 865: 862: 861: 851: 850: 844: 840: 839: 836: 835: 829: 828: 822: 819: 818: 810: 809: 803: 797: 796: 793: 792: 784: 783: 777: 774: 773: 765: 764: 758: 752: 751: 748: 747: 739: 738: 732: 729: 728: 720: 719: 713: 707: 706: 701: 696: 692: 691: 681: 680: 677: 676: 665: 664: 662: 661: 656: 651: 645: 643: 639: 638: 636: 635: 630: 625: 619: 617: 613: 612: 610: 609: 604: 598: 596: 592: 591: 581: 580: 577: 576: 573: 572: 564: 563: 552: 546: 545: 542: 541: 533: 532: 529: 528: 526: 525: 521: 517: 513: 509: 508:tail of embryo 505: 501: 497: 493: 489: 485: 482: 481: 470: 467: 466: 464: 463: 459: 455: 451: 447: 443: 439: 435: 431: 427: 423: 420: 419: 407: 406: 398: 387: 381: 380: 377:RNA expression 369: 368: 365: 364: 356: 352: 351: 343: 340: 335: 329: 328: 319: 312: 306: 302: 301: 296: 290: 289: 281: 280: 268: 267: 264: 263: 255: 251: 250: 242: 239: 234: 228: 227: 218: 211: 205: 201: 200: 193: 187: 186: 178: 177: 165: 164: 121: 117: 116: 108: 100: 99: 95: 94: 91: 90: 87: 86: 76: 75: 67: 66: 55: 49: 48: 40: 39: 31: 30: 15: 13: 10: 9: 6: 4: 3: 2: 2859: 2848: 2845: 2844: 2842: 2825: 2819: 2814: 2810: 2801: 2796: 2794: 2789: 2787: 2782: 2781: 2778: 2771: 2767: 2766: 2761: 2757: 2753: 2752: 2748: 2741: 2737: 2732: 2727: 2723: 2719: 2715: 2710: 2706: 2702: 2697: 2692: 2688: 2684: 2681:(9): 958–63. 2680: 2676: 2672: 2667: 2663: 2659: 2654: 2649: 2645: 2641: 2637: 2632: 2628: 2624: 2619: 2614: 2610: 2606: 2602: 2598: 2594: 2589: 2585: 2581: 2576: 2571: 2567: 2563: 2559: 2554: 2550: 2546: 2542: 2538: 2534: 2530: 2527:(2): 165–70. 2526: 2522: 2516: 2512: 2508: 2503: 2498: 2494: 2490: 2486: 2482: 2478: 2473: 2469: 2465: 2460: 2455: 2452:(1): 136–41. 2451: 2447: 2443: 2438: 2434: 2430: 2425: 2420: 2416: 2412: 2408: 2403: 2399: 2395: 2390: 2385: 2381: 2377: 2373: 2369: 2365: 2360: 2356: 2352: 2347: 2342: 2338: 2334: 2330: 2325: 2321: 2317: 2312: 2307: 2303: 2299: 2296:(5): 1400–5. 2295: 2291: 2287: 2282: 2278: 2274: 2269: 2264: 2260: 2256: 2252: 2248: 2244: 2239: 2235: 2231: 2227: 2223: 2219: 2215: 2212:(6): 479–82. 2211: 2207: 2202: 2201: 2196: 2187: 2183: 2178: 2173: 2169: 2165: 2161: 2154: 2152: 2148: 2143: 2139: 2134: 2129: 2125: 2121: 2117: 2110: 2107: 2102: 2098: 2093: 2088: 2085:(1): 136–41. 2084: 2080: 2076: 2069: 2067: 2063: 2058: 2054: 2050: 2046: 2042: 2038: 2035:(2): 165–70. 2034: 2030: 2022: 2019: 2014: 2010: 2005: 2000: 1996: 1992: 1988: 1984: 1980: 1973: 1971: 1969: 1967: 1965: 1961: 1956: 1952: 1947: 1942: 1938: 1934: 1930: 1923: 1921: 1919: 1917: 1913: 1908: 1904: 1899: 1894: 1890: 1886: 1883:(5): 1306–8. 1882: 1878: 1874: 1866: 1863: 1858: 1854: 1849: 1844: 1840: 1836: 1833:(5): 1400–5. 1832: 1828: 1824: 1817: 1815: 1811: 1806: 1802: 1798: 1794: 1790: 1786: 1782: 1778: 1771: 1768: 1757: 1756:www.abcam.com 1753: 1747: 1745: 1741: 1736: 1732: 1727: 1722: 1718: 1714: 1710: 1706: 1702: 1695: 1693: 1689: 1684: 1680: 1675: 1670: 1667:(2): 249–62. 1666: 1662: 1658: 1651: 1648: 1643: 1639: 1634: 1629: 1625: 1621: 1617: 1610: 1608: 1606: 1604: 1600: 1589: 1585: 1579: 1577: 1573: 1562: 1558: 1552: 1549: 1544: 1540: 1535: 1530: 1525: 1520: 1516: 1512: 1508: 1501: 1498: 1493: 1489: 1484: 1479: 1476:(2): 249–62. 1475: 1471: 1467: 1460: 1458: 1454: 1449: 1443: 1441: 1437: 1432: 1428: 1423: 1418: 1414: 1410: 1407:(5): 1306–8. 1406: 1402: 1398: 1390: 1387: 1382: 1378: 1373: 1368: 1364: 1360: 1356: 1349: 1346: 1341: 1337: 1331: 1328: 1323: 1319: 1313: 1310: 1306: 1302: 1297: 1295: 1293: 1289: 1285: 1281: 1276: 1274: 1272: 1268: 1261: 1256: 1253: 1250: 1247: 1245: 1242: 1239: 1236: 1233: 1230: 1229: 1228: 1226: 1218: 1212: 1209: 1206: 1202: 1198: 1195: 1191: 1187: 1186: 1182: 1180: 1178: 1174: 1170: 1165: 1159: 1157: 1147: 1145: 1143: 1138: 1136: 1135:ubiquitinated 1131: 1125: 1123: 1120: 1114: 1112: 1106: 1104: 1102: 1098: 1094: 1090: 1086: 1082: 1078: 1074: 1070: 1066: 1062: 1058: 1053: 1051: 1047: 1043: 1039: 1035: 1031: 1027: 1023: 1019: 1016: 1012: 1008: 996: 991: 987: 983: 980: 976: 969: 967: 964: 960: 956: 952: 949: 945: 941: 934: 928: 924: 921: 915: 913: 907: 903: 900: 896: 889: 887: 883: 879: 873: 869: 866: 860: 858: 852: 848: 845: 843:RefSeq (mRNA) 841: 834: 830: 826: 823: 817: 816: 811: 807: 804: 802: 798: 791: 790: 785: 781: 778: 772: 771: 766: 762: 759: 757: 753: 746: 745: 740: 736: 733: 727: 726: 721: 717: 714: 712: 708: 705: 702: 700: 697: 693: 690: 686: 682: 675: 671: 666: 660: 657: 655: 652: 650: 647: 646: 644: 641: 640: 634: 631: 629: 626: 624: 621: 620: 618: 615: 614: 608: 605: 603: 600: 599: 597: 594: 593: 590: 589:Gene ontology 586: 582: 570: 565: 561: 556: 553: 551: 547: 539: 534: 523: 520:visual cortex 519: 515: 511: 507: 503: 499: 495: 491: 487: 486: 483: 479: 474: 471: 461: 457: 453: 449: 445: 441: 437: 433: 429: 425: 424: 421: 417: 412: 409: 408: 405: 403: 399: 397: 396: 392: 391: 388: 386: 382: 378: 374: 370: 362: 357: 353: 349: 344: 334: 330: 323: 316: 310: 303: 295: 291: 287: 282: 278: 273: 269: 261: 256: 252: 248: 243: 233: 229: 222: 215: 209: 202: 198: 192: 188: 184: 179: 175: 170: 166: 162: 158: 154: 150: 146: 142: 138: 134: 130: 126: 118: 113: 106: 101: 96: 85: 83: 77: 72: 69: 68: 64: 61: 54: 50: 45: 41: 37: 32: 27: 22: 2823: 2763: 2721: 2717: 2678: 2674: 2643: 2639: 2600: 2596: 2565: 2561: 2524: 2520: 2484: 2480: 2449: 2445: 2414: 2410: 2371: 2367: 2339:(4): 423–9. 2336: 2332: 2293: 2289: 2253:(4): 940–4. 2250: 2246: 2209: 2205: 2167: 2163: 2123: 2119: 2109: 2082: 2078: 2032: 2028: 2021: 1986: 1982: 1936: 1932: 1880: 1876: 1865: 1830: 1826: 1783:(3): 71–82. 1780: 1777:Reproduction 1776: 1770: 1759:. Retrieved 1755: 1708: 1704: 1664: 1660: 1650: 1626:(4): 423–9. 1623: 1619: 1591:. Retrieved 1587: 1564:. Retrieved 1560: 1551: 1514: 1510: 1500: 1473: 1469: 1404: 1400: 1389: 1362: 1358: 1348: 1339: 1330: 1321: 1312: 1222: 1219:Interactions 1201:Gene Mapping 1190:Western Blot 1183:Applications 1166: 1163: 1151: 1139: 1132: 1129: 1121: 1118: 1110: 1054: 1014: 1006: 1005: 930: 909: 882:NM_001163820 878:NM_001163819 875: 854: 832: 813: 787: 768: 742: 723: 703: 698: 400: 393: 120:External IDs 79: 2806:PDB gallery 1534:2434/618936 633:nucleoplasm 454:skin of leg 359:28,545,546 346:28,532,493 258:35,467,104 245:35,452,338 98:Identifiers 1761:2018-11-09 1593:2018-11-09 1566:2018-11-09 1307:, May 2017 1286:, May 2017 1262:References 659:DNA repair 404:(ortholog) 141:HomoloGene 1805:249432754 1040:, FANCE, 912:NP_068741 886:NM_028348 857:NM_021922 689:Orthologs 149:GeneCards 2841:Category 2740:16127171 2705:16116422 2662:15502827 2627:15199141 2584:15115758 2549:10149290 2541:12973351 2511:12724401 2468:12649160 2433:12239156 2398:12093742 2355:11157805 2320:10205272 2234:23242981 2186:15262960 2142:15115758 2101:12649160 2057:10149290 2049:12973351 2013:12093742 1955:12239156 1907:11001585 1857:10205272 1797:35671285 1735:17308347 1683:11239454 1642:11157805 1543:27986371 1492:11239454 1431:11001585 1303:– 1282:– 1225:interact 1214:nucleus. 1173:prophase 1160:Function 979:Wikidata 668:Sources: 524:epiblast 458:testicle 2770:PDBe-KB 2760:UniProt 2696:2704909 2311:1377877 2277:9382107 2268:1715980 2226:9147877 1898:1288571 1848:1377877 1726:1865054 1422:1288571 1381:7662964 1305:Ensembl 1284:Ensembl 1227:with: 1203:, here 1177:meiosis 1169:oocytes 1142:epitope 1097:meiotic 1057:nuclear 1011:protein 801:UniProt 756:Ensembl 695:Species 674:QuickGO 628:nucleus 379:pattern 237:6p21.31 137:1920025 105:Aliases 2765:Q9HB96 2738:  2703:  2693:  2660:  2625:  2618:480901 2615:  2582:  2547:  2539:  2509:  2502:164758 2499:  2466:  2431:  2396:  2389:125396 2386:  2353:  2318:  2308:  2275:  2265:  2232:  2224:  2184:  2140:  2099:  2055:  2047:  2011:  2004:125396 2001:  1953:  1905:  1895:  1855:  1845:  1803:  1795:  1733:  1723:  1681:  1640:  1541:  1490:  1429:  1419:  1379:  1238:FANCD2 1073:FANCD2 1048:, and 1038:FANCD2 1034:FANCD1 965:search 963:PubMed 815:Q9HB96 711:Entrez 550:BioGPS 512:morula 500:embryo 496:embryo 430:oocyte 129:613976 21:France 2545:S2CID 2446:Blood 2411:Blood 2230:S2CID 2079:Blood 2053:S2CID 1933:Blood 1801:S2CID 1359:Blood 1255:FANCC 1251:, and 1249:FANCG 1244:FANCF 1232:FANCA 1194:IHC-P 1175:I of 1085:BRCA1 1081:FANCC 1069:FANCG 1065:FANCF 1061:FANCC 1050:FANCL 1046:FANCG 1042:FANCF 1030:FANCC 1026:FANCB 1022:FANCA 1015:FANCE 1009:is a 744:72775 704:Mouse 699:Human 670:Amigo 438:gonad 402:Mouse 395:Human 342:Start 277:Mouse 241:Start 174:Human 153:FANCE 145:11066 112:FANCE 29:FANCE 2824:2ilr 2758:for 2736:PMID 2701:PMID 2658:PMID 2623:PMID 2580:PMID 2537:PMID 2507:PMID 2464:PMID 2429:PMID 2394:PMID 2351:PMID 2316:PMID 2273:PMID 2222:PMID 2182:PMID 2138:PMID 2097:PMID 2045:PMID 2009:PMID 1951:PMID 1903:PMID 1853:PMID 1793:PMID 1731:PMID 1679:PMID 1638:PMID 1539:PMID 1488:PMID 1427:PMID 1377:PMID 1192:and 1067:and 1018:gene 725:2178 385:Bgee 333:Band 294:Chr. 232:Band 191:Chr. 125:OMIM 82:2ILR 63:RCSB 60:PDBe 2756:PDB 2726:doi 2722:280 2691:PMC 2683:doi 2648:doi 2613:PMC 2605:doi 2570:doi 2529:doi 2497:PMC 2489:doi 2454:doi 2450:102 2419:doi 2415:100 2384:PMC 2376:doi 2341:doi 2306:PMC 2298:doi 2263:PMC 2255:doi 2214:doi 2172:doi 2168:279 2128:doi 2087:doi 2083:102 2037:doi 1999:PMC 1991:doi 1941:doi 1937:100 1893:PMC 1885:doi 1843:PMC 1835:doi 1785:doi 1781:164 1721:PMC 1713:doi 1669:doi 1628:doi 1529:hdl 1519:doi 1478:doi 1417:PMC 1409:doi 1367:doi 1095:of 932:n/a 833:n/a 492:lip 355:End 254:End 157:OMA 133:MGI 53:PDB 2843:: 2762:: 2734:. 2720:. 2716:. 2699:. 2689:. 2679:37 2677:. 2673:. 2656:. 2644:36 2642:. 2638:. 2621:. 2611:. 2601:24 2599:. 2595:. 2578:. 2566:13 2564:. 2560:. 2543:. 2535:. 2525:35 2523:. 2505:. 2495:. 2485:23 2483:. 2479:. 2462:. 2448:. 2444:. 2427:. 2413:. 2409:. 2392:. 2382:. 2372:21 2370:. 2366:. 2349:. 2337:10 2335:. 2331:. 2314:. 2304:. 2294:64 2292:. 2288:. 2271:. 2261:. 2251:61 2249:. 2245:. 2228:. 2220:. 2210:50 2208:. 2180:. 2166:. 2162:. 2150:^ 2136:. 2124:13 2122:. 2118:. 2095:. 2081:. 2077:. 2065:^ 2051:. 2043:. 2033:35 2031:. 2007:. 1997:. 1987:21 1985:. 1981:. 1963:^ 1949:. 1935:. 1931:. 1915:^ 1901:. 1891:. 1881:67 1879:. 1875:. 1851:. 1841:. 1831:64 1829:. 1825:. 1813:^ 1799:. 1791:. 1779:. 1754:. 1743:^ 1729:. 1719:. 1709:35 1707:. 1703:. 1691:^ 1677:. 1663:. 1659:. 1636:. 1624:10 1622:. 1618:. 1602:^ 1586:. 1575:^ 1559:. 1537:. 1527:. 1515:65 1513:. 1509:. 1486:. 1472:. 1468:. 1456:^ 1439:^ 1425:. 1415:. 1405:67 1403:. 1399:. 1375:. 1363:86 1361:. 1357:. 1338:. 1320:. 1291:^ 1270:^ 1154:10 1063:, 1055:A 1044:, 1032:, 1028:, 1024:, 672:/ 361:bp 348:bp 260:bp 247:bp 155:; 151:: 147:; 143:: 139:; 135:: 131:; 127:: 2799:e 2792:t 2785:v 2772:. 2742:. 2728:: 2707:. 2685:: 2664:. 2650:: 2629:. 2607:: 2586:. 2572:: 2551:. 2531:: 2513:. 2491:: 2470:. 2456:: 2435:. 2421:: 2400:. 2378:: 2357:. 2343:: 2322:. 2300:: 2279:. 2257:: 2236:. 2216:: 2188:. 2174:: 2144:. 2130:: 2103:. 2089:: 2059:. 2039:: 2015:. 1993:: 1957:. 1943:: 1909:. 1887:: 1859:. 1837:: 1807:. 1787:: 1764:. 1737:. 1715:: 1685:. 1671:: 1665:7 1644:. 1630:: 1596:. 1569:. 1545:. 1531:: 1521:: 1494:. 1480:: 1474:7 1450:. 1433:. 1411:: 1383:. 1369:: 1342:. 1324:. 1257:. 1240:, 1234:, 279:) 176:) 159:: 23:.

Index

France

PDB
PDBe
RCSB
2ILR
Aliases
FANCE
OMIM
613976
MGI
1920025
HomoloGene
11066
GeneCards
FANCE
OMA
FANCE - orthologs
Human
Chromosome 6 (human)
Chr.
Chromosome 6 (human)
Chromosome 6 (human)
Genomic location for FANCE
Genomic location for FANCE
Band
bp
bp
Mouse
Chromosome 17 (mouse)

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