Knowledge (XXG)

Atrophin 1

Source πŸ“

242: 219: 116: 141: 493: 500: 507: 248: 147: 1003:. The encoded protein includes a serine repeat and a region of alternating acidic and basic amino acids, as well as the variable glutamine repeat. The function of Atrophin-1 has not yet been determined. There is evidence provided by studies of Atrophin-1 in animals to suggest it acts as a transcriptional 2362:
Dias Neto E, Correa RG, Verjovski-Almeida S, Briones MR, Nagai MA, da Silva W, Zago MA, Bordin S, Costa FF, Goldman GH, Carvalho AF, Matsukuma A, Baia GS, Simpson DH, Brunstein A, de Oliveira PS, Bucher P, Jongeneel CV, O'Hare MJ, Soares F, Brentani RR, Reis LF, de Souza SJ, Simpson AJ (March 2000).
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In patients with DRPLA, truncated ATN1 has been observed forming intranuclear aggregates that cause cell death. The symptoms of this disorder can be credited to the significant reduction of brain and spinal tissue observed in those afflicted with DRPLA. There are both juvenile-onset and late
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Hayashi Y, Kakita A, Yamada M, Koide R, Igarashi S, Takano H, Ikeuchi T, Wakabayashi K, Egawa S, Tsuji S, Takahashi H (December 1998). "Hereditary dentatorubral-pallidoluysian atrophy: detection of widespread ubiquitinated neuronal and glial intranuclear inclusions in the brain".
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The ATN1 gene has a segment of DNA called the CAG trinucleotide repeat. It is made up of cytosine, adenine, and guanine. The number of CAG repeats in the ATN1 gene in a healthy person will range from six to thirty-five repeats. CAG repeats that exceed thirty-five can cause a
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Yanagisawa H, Fujii K, Nagafuchi S, Nakahori Y, Nakagome Y, Akane A, Nakamura M, Sano A, Komure O, Kondo I, Jin DK, SΓΈrensen SA, Potter NT, Young SR, Nakamura K, Nukina N, Nagao Y, Tadokoro K, Okuyama T, Miyashita T, Inoue T, Kanazawa I, Yamada M (March 1996).
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Wellington CL, Ellerby LM, Hackam AS, Margolis RL, Trifiro MA, Singaraja R, McCutcheon K, Salvesen GS, Propp SS, Bromm M, Rowland KJ, Zhang T, Rasper D, Roy S, Thornberry N, Pinsky L, Kakizuka A, Ross CA, Nicholson DW, Bredesen DE, Hayden MR (April 1998).
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Nagafuchi S, Yanagisawa H, Sato K, Shirayama T, Ohsaki E, Bundo M, Takeda T, Tadokoro K, Kondo I, Murayama N (January 1994). "Dentatorubral and pallidoluysian atrophy expansion of an unstable CAG trinucleotide on chromosome 12p".
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Nagafuchi S, Yanagisawa H, Ohsaki E, Shirayama T, Tadokoro K, Inoue T, Yamada M (October 1994). "Structure and expression of the gene responsible for the triplet repeat disorder, dentatorubral and pallidoluysian atrophy (DRPLA)".
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Koide R, Ikeuchi T, Onodera O, Tanaka H, Igarashi S, Endo K, Takahashi H, Kondo R, Ishikawa A, Hayashi T (January 1994). "Unstable expansion of CAG repeat in hereditary dentatorubral-pallidoluysian atrophy (DRPLA)".
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Burke JR, Wingfield MS, Lewis KE, Roses AD, Lee JE, Hulette C, Pericak-Vance MA, Vance JM (August 1994). "The Haw River syndrome: dentatorubropallidoluysian atrophy (DRPLA) in an African-American family".
2294:"Single sperm analysis of the CAG repeats in the gene for dentatorubral-pallidoluysian atrophy (DRPLA): the instability of the CAG repeats in the DRPLA gene is prominent among the CAG repeat diseases" 1048:(NES). It has been shown that a mutation of the NES in ATN1 can change where ATN1 localizes, and can cause aggregation to occur in the nucleus. This can lead to an increase in cellular toxicity. 1044:
in ATN1. Studies have supported the idea that mutated Atrophin-1 gathers in neurons and disrupts cell function. The sequence of the ATN1 gene contains a nuclear localizing signal (NLS) and a
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Takano T, Yamanouchi Y, Nagafuchi S, Yamada M (February 1996). "Assignment of the dentatorubral and pallidoluysian atrophy (DRPLA) gene to 12p 13.31 by fluorescence in situ hybridization".
2329:"Dentatorubral-pallidoluysian atrophy protein interacts through a proline-rich region near polyglutamine with the SH3 domain of an insulin receptor tyrosine kinase substrate" 1529:"Dentatorubral-pallidoluysian atrophy protein interacts through a proline-rich region near polyglutamine with the SH3 domain of an insulin receptor tyrosine kinase substrate" 1746:
Yazawa I, Nukina N, Hashida H, Goto J, Yamada M, Kanazawa I (May 1995). "Abnormal gene product identified in hereditary dentatorubral-pallidoluysian atrophy (DRPLA) brain".
255: 154: 725: 706: 77: 1272:"Atrophin-1, the dentato-rubral and pallido-luysian atrophy gene product, interacts with ETO/MTG8 in the nuclear matrix and represses transcription" 2178:"Caspase cleavage of gene products associated with triplet expansion disorders generates truncated fragments containing the polyglutamine tract" 1713:"Molecular cloning of a full-length cDNA for dentatorubral-pallidoluysian atrophy and regional expressions of the expanded alleles in the CNS" 2502: 1204: 1186: 1056: 2507: 241: 940: 2474: 933: 218: 1251: 1173: 1152: 1019:
The function of Atrophin-1 has not been defined yet. It is widely hypothesized that Atrophin-1 functions as a transcriptional
140: 115: 1169: 2480: 2418:"Protein binding of a DRPLA family through arginine-glutamic acid dipeptide repeats is enhanced by extended polyglutamine" 1624:"Protein binding of a DRPLA family through arginine-glutamic acid dipeptide repeats is enhanced by extended polyglutamine" 1052: 1148: 57: 1092: 2211:
Wood JD, Yuan J, Margolis RL, Colomer V, Duan K, Kushi J, Kaminsky Z, Kleiderlein JJ, Sharp AH, Ross CA (June 1998).
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Wood JD, Yuan J, Margolis RL, Colomer V, Duan K, Kushi J, Kaminsky Z, Kleiderlein JJ, Sharp AH, Ross CA (June 1998).
254: 153: 247: 146: 2467: 2107:"Large-scale sequencing in human chromosome 12p13: experimental and computational gene structure determination" 1270:
Wood JD, Nucifora FC, Duan K, Zhang C, Wang J, Kim Y, Schilling G, Sacchi N, Liu JM, Ross CA (September 2000).
770: 65: 751: 2458: 1045: 129: 1007:. Atrophin-1 can be found in the nuclear and cytoplasmic compartments of neurons. It is expressed in 2376: 1937:"Novel triplet repeat containing genes in human brain: cloning, expression, and length polymorphisms" 44: 2486: 1972:"A gene-rich cluster between the CD4 and triosephosphate isomerase genes at human chromosome 12p13" 1028: 891: 844: 2213:"Atrophin-1, the DRPLA gene product, interacts with two families of WW domain-containing proteins" 2070:
Margolis RL, Li SH, Young WS, Wagster MV, Stine OC, Kidwai AS, Ashworth RG, Ross CA (March 1996).
1575:"Atrophin-1, the DRPLA gene product, interacts with two families of WW domain-containing proteins" 1059:" or "dentatorubropallidoluysian atrophy". Dentatorubral-pallidoluysian atrophy (DRPLA) is a rare 2280: 2242: 1923: 1885: 1847: 1809: 1771: 1604: 1358: 1068: 89: 2416:
Yanagisawa H, Bundo M, Miyashita T, Okamura-Oho Y, Tadokoro K, Tokunaga K, Yamada M (May 2000).
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Yanagisawa H, Bundo M, Miyashita T, Okamura-Oho Y, Tadokoro K, Tokunaga K, Yamada M (May 2000).
916: 895: 865: 840: 2142:"Dentatorubral pallidoluysian atrophy (DRPLA) protein is cleaved by caspase-3 during apoptosis" 2439: 2404: 2350: 2315: 2272: 2234: 2199: 2163: 2128: 2093: 2058: 2022: 1993: 1958: 1915: 1877: 1839: 1801: 1763: 1734: 1699: 1645: 1596: 1550: 1482: 1432: 1350: 1301: 1083:
adult-onset variants of DRPLA, which show differing degrees of severity of specific symptoms.
1064: 1060: 37: 2429: 2394: 2384: 2340: 2305: 2264: 2224: 2189: 2153: 2118: 2083: 2048: 2037:"A unique origin and multistep process for the generation of expanded DRPLA triplet repeats" 2014: 1983: 1970:
Ansari-Lari MA, Muzny DM, Lu J, Lu F, Lilley CE, Spanos S, Malley T, Gibbs RA (April 1996).
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is a protein that indirectly suppresses the activity of specific genes by interacting with
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Takiyama Y, Sakoe K, Amaike M, Soutome M, Ogawa T, Nakano I, Nishizawa M (March 1999).
1729: 1712: 1694: 1669: 1477: 1460: 1296: 1271: 1079:. The disorder is related to the expansion of a trinucleotide repeat within this gene. 1008: 2463: 640: 635: 630: 625: 620: 604: 599: 594: 589: 584: 579: 563: 558: 553: 548: 2496: 2399: 2364: 2088: 2071: 1670:"Histone deacetylase-associating Atrophin proteins are nuclear receptor corepressors" 535: 2284: 2246: 1927: 1889: 1851: 1608: 1362: 1813: 1775: 1385: 1024: 1020: 1004: 327: 106: 69: 1503: 93: 2365:"Shotgun sequencing of the human transcriptome with ORF expressed sequence tags" 1461:"Pathological accumulation of atrophin-1 in dentatorubralpallidoluysian atrophy" 1209:
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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Proceedings of the National Academy of Sciences of the United States of America
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Onodera O, Oyake M, Takano H, Ikeuchi T, Igarashi S, Tsuji S (November 1995).
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Miyashita T, Okamura-Oho Y, Mito Y, Nagafuchi S, Yamada M (November 1997).
2018: 1953: 1936: 1703: 1649: 1640: 1623: 1591: 1574: 1554: 1486: 1436: 1427: 1410: 1354: 1305: 2345: 2328: 2319: 2310: 2293: 2276: 2268: 2238: 2203: 2167: 2132: 2097: 2062: 2053: 2036: 2026: 1997: 1962: 1919: 1881: 1843: 1805: 1767: 1738: 1600: 1545: 1528: 1287: 980: 975: 1227: 1076: 1041: 964: 815: 796: 1685: 1321:"Atrophins' emerging roles in development and neurodegenerative disease" 2123: 2106: 1988: 1971: 1835: 1797: 996: 782: 737: 1873: 1759: 2072:"DRPLA gene (atrophin-1) sequence and mRNA expression in human brain" 1935:
Li SH, McInnis MG, Margolis RL, Antonarakis SE, Ross CA (June 1993).
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Shen Y, Lee G, Choe Y, Zoltewicz JS, Peterson AS (February 2007).
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Ansari-Lari MA, Shen Y, Muzny DM, Lee W, Gibbs RA (March 1997).
1123: 1117: 1000: 61: 515: 1228:"ATN1 atrophin 1 [Homo sapiens (human)] - Gene - NCBI" 1668:
Wang L, Rajan H, Pitman JL, McKeown M, Tsai CC (March 2006).
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International Journal of Clinical and Experimental Pathology
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Okamura-Oho Y, Miyashita T, Ohmi K, Yamada M (June 1999).
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Okamura-Oho Y, Miyashita T, Ohmi K, Yamada M (June 1999).
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negative regulation of transcription by RNA polymerase II
317: 482: 48:, B37, D12S755E, DRPLA, HRS, NOD, atrophin 1, CHEDDA 909: 884: 858: 833: 437:
dentate gyrus of hippocampal formation granule cell
1165: 1163: 1161: 1144: 1142: 1140: 264: 163: 1051:Mutations in ATN1 are associated with a form of 1568: 1566: 1564: 1454: 1452: 1450: 1448: 1446: 1170:GRCm38: Ensembl release 89: ENSMUSG00000004263 1504:"Dentatorubral-Pallidoluysian Atrophy, DRPLA" 1222: 1220: 1218: 8: 1265: 1263: 1261: 1149:GRCh38: Ensembl release 89: ENSG00000111676 666: 631:regulation of transcription, DNA-templated 531: 305: 204: 101: 2466:at the U.S. National Library of Medicine 2433: 2398: 2388: 2344: 2309: 2228: 2193: 2157: 2122: 2087: 2052: 1987: 1952: 1728: 1693: 1639: 1590: 1544: 1476: 1426: 1344: 1295: 2076:Brain Research. Molecular Brain Research 1136: 2459:GeneReviews/NCBI/NIH/UW entry on DRPLA 1411:"Functional architecture of atrophins" 999:that in humans is encoded by the ATN1 18: 1380: 1378: 1376: 1374: 1372: 1319:Shen Y, Peterson AS (February 2009). 269: 230: 225: 168: 127: 122: 7: 2217:Molecular and Cellular Neurosciences 1579:Molecular and Cellular Neurosciences 1325:Cellular and Molecular Life Sciences 1057:dentatorubral-pallidoluysian atrophy 2182:The Journal of Biological Chemistry 2146:The Journal of Biological Chemistry 1415:The Journal of Biological Chemistry 1717:American Journal of Human Genetics 906: 881: 855: 830: 806: 787: 761: 742: 716: 697: 626:central nervous system development 554:transcription corepressor activity 487: 405: 343: 322: 14: 1459:Suzuki Y, Yazawa I (April 2011). 505: 498: 491: 253: 246: 240: 217: 152: 145: 139: 114: 585:perinuclear region of cytoplasm 559:protein domain specific binding 1508:themedicalbiochemistrypage.org 1252:"Entrez Gene: ATN1 atrophin 1" 516:More reference expression data 471:More reference expression data 359:right hemisphere of cerebellum 1: 1053:trinucleotide repeat disorder 238: 137: 2503:Genes on human chromosome 12 2089:10.1016/0169-328X(95)00241-J 641:transcription, DNA-templated 1276:The Journal of Cell Biology 379:right lobe of thyroid gland 2524: 2508:Transcription coregulators 2485:gene details page in the 1063:disorder characterized by 383:left lobe of thyroid gland 1337:10.1007/s00018-008-8403-9 1205:"Mouse PubMed Reference:" 1187:"Human PubMed Reference:" 1042:gain-of-function mutation 979: 974: 970: 963: 947: 941:Chr 6: 124.72 – 124.73 Mb 928: 913: 888: 877: 862: 837: 826: 813: 809: 794: 790: 781: 768: 764: 749: 745: 736: 723: 719: 704: 700: 691: 676: 669: 665: 649: 534: 530: 513: 490: 481: 468: 417: 408: 355: 346: 316: 308: 304: 287: 274: 237: 216: 207: 203: 186: 173: 136: 113: 104: 100: 55: 52: 42: 35: 30: 26: 21: 2468:Medical Subject Headings 2422:Human Molecular Genetics 2333:Human Molecular Genetics 2298:Human Molecular Genetics 2159:10.1074/jbc.272.46.29238 2041:Human Molecular Genetics 1628:Human Molecular Genetics 1533:Human Molecular Genetics 621:neuron apoptotic process 2195:10.1074/jbc.273.15.9158 1674:Genes & Development 1390:Genetics Home Reference 1091:ATN1 has been shown to 16:Protein found in humans 2390:10.1073/pnas.97.7.3491 2230:10.1006/mcne.1998.0677 2019:10.1006/geno.1996.0100 1954:10.1006/geno.1993.1232 1592:10.1006/mcne.1998.0677 1428:10.1074/jbc.M610274200 934:Chr 12: 6.92 – 6.94 Mb 429:superior frontal gyrus 421:neural layer of retina 2269:10.1007/s004010050933 2257:Acta Neuropathologica 1288:10.1083/jcb.150.5.939 1046:nuclear export signal 1035:Clinical significance 425:primary visual cortex 130:Chromosome 12 (human) 2479:genome location and 2435:10.1093/hmg/9.9.1433 1641:10.1093/hmg/9.9.1433 1232:www.ncbi.nlm.nih.gov 1029:DNA-binding proteins 1023:. A transcriptional 271:6 F2|6 59.17 cM 232:Chromosome 6 (mouse) 2487:UCSC Genome Browser 2381:2000PNAS...97.3491D 2346:10.1093/hmg/8.6.947 2311:10.1093/hmg/8.3.453 2054:10.1093/hmg/5.3.373 1686:10.1101/gad.1393506 1546:10.1093/hmg/8.6.947 395:canal of the cervix 2124:10.1101/gr.7.3.268 1989:10.1101/gr.6.4.314 1836:10.1038/ng0894-521 1798:10.1038/ng1094-177 1069:myoclonic epilepsy 771:ENSMUSG00000004263 614:Biological process 573:Cellular component 542:Molecular function 371:right uterine tube 363:anterior pituitary 1874:10.1038/ng0194-14 1760:10.1038/ng0595-99 1065:cerebellar ataxia 1061:neurodegenerative 990: 989: 986: 985: 959: 958: 924: 923: 903: 902: 873: 872: 852: 851: 822: 821: 803: 802: 777: 776: 758: 757: 732: 731: 713: 712: 661: 660: 526: 525: 522: 521: 477: 476: 464: 463: 441:cerebellar cortex 402: 401: 300: 299: 199: 198: 2515: 2447: 2437: 2412: 2402: 2392: 2358: 2348: 2323: 2313: 2288: 2250: 2232: 2207: 2197: 2171: 2161: 2152:(46): 29238–42. 2136: 2126: 2101: 2091: 2066: 2056: 2030: 2001: 1991: 1966: 1956: 1931: 1912:10.1038/ng0194-9 1893: 1855: 1817: 1779: 1742: 1732: 1707: 1697: 1654: 1653: 1643: 1619: 1613: 1612: 1594: 1570: 1559: 1558: 1548: 1524: 1518: 1517: 1515: 1514: 1500: 1491: 1490: 1480: 1456: 1441: 1440: 1430: 1406: 1400: 1399: 1397: 1396: 1382: 1367: 1366: 1348: 1316: 1310: 1309: 1299: 1267: 1256: 1255: 1248: 1242: 1241: 1239: 1238: 1224: 1213: 1212: 1201: 1195: 1194: 1183: 1177: 1167: 1156: 1146: 972: 971: 943: 936: 919: 907: 898: 882: 878:RefSeq (protein) 868: 856: 847: 831: 807: 788: 762: 743: 717: 698: 667: 532: 518: 509: 502: 495: 488: 473: 453:ventricular zone 433:genital tubercle 413: 411:Top expressed in 406: 351: 349:Top expressed in 344: 323: 306: 296: 283: 272: 257: 250: 244: 233: 221: 205: 195: 182: 171: 156: 149: 143: 132: 118: 102: 96: 94:ATN1 - orthologs 47: 40: 19: 2523: 2522: 2518: 2517: 2516: 2514: 2513: 2512: 2493: 2492: 2455: 2450: 2415: 2361: 2326: 2291: 2253: 2210: 2188:(15): 9158–67. 2174: 2139: 2111:Genome Research 2104: 2069: 2033: 2004: 1976:Genome Research 1969: 1934: 1900:Nature Genetics 1896: 1862:Nature Genetics 1858: 1824:Nature Genetics 1820: 1786:Nature Genetics 1782: 1748:Nature Genetics 1745: 1710: 1667: 1663: 1661:Further reading 1658: 1657: 1621: 1620: 1616: 1572: 1571: 1562: 1526: 1525: 1521: 1512: 1510: 1502: 1501: 1494: 1458: 1457: 1444: 1408: 1407: 1403: 1394: 1392: 1384: 1383: 1370: 1318: 1317: 1313: 1269: 1268: 1259: 1250: 1249: 1245: 1236: 1234: 1226: 1225: 1216: 1203: 1202: 1198: 1185: 1184: 1180: 1168: 1159: 1147: 1138: 1133: 1089: 1073:choreoathetosis 1037: 1017: 981:View/Edit Mouse 976:View/Edit Human 939: 932: 929:Location (UCSC) 915: 894: 890: 864: 843: 839: 752:ENSG00000111676 645: 609: 568: 549:protein binding 514: 504: 503: 497: 496: 469: 460: 455: 451: 447: 445:muscle of thigh 443: 439: 435: 431: 427: 423: 409: 398: 393: 389: 385: 381: 377: 373: 369: 365: 361: 347: 291: 278: 270: 260: 259: 258: 251: 231: 208:Gene location ( 190: 177: 169: 159: 158: 157: 150: 128: 105:Gene location ( 56: 43: 36: 17: 12: 11: 5: 2521: 2519: 2511: 2510: 2505: 2495: 2494: 2491: 2490: 2471: 2461: 2454: 2453:External links 2451: 2449: 2448: 2428:(9): 1433–42. 2413: 2359: 2324: 2289: 2251: 2208: 2172: 2137: 2102: 2067: 2031: 2002: 1967: 1932: 1894: 1856: 1818: 1780: 1743: 1723:(5): 1050–60. 1708: 1664: 1662: 1659: 1656: 1655: 1634:(9): 1433–42. 1614: 1560: 1519: 1492: 1442: 1421:(7): 5037–44. 1401: 1368: 1311: 1257: 1243: 1214: 1196: 1178: 1157: 1135: 1134: 1132: 1129: 1128: 1127: 1121: 1115: 1109: 1103: 1088: 1085: 1036: 1033: 1016: 1013: 1009:nervous tissue 988: 987: 984: 983: 978: 968: 967: 961: 960: 957: 956: 954: 952: 945: 944: 937: 930: 926: 925: 922: 921: 911: 910: 904: 901: 900: 886: 885: 879: 875: 874: 871: 870: 860: 859: 853: 850: 849: 835: 834: 828: 824: 823: 820: 819: 811: 810: 804: 801: 800: 792: 791: 785: 779: 778: 775: 774: 766: 765: 759: 756: 755: 747: 746: 740: 734: 733: 730: 729: 721: 720: 714: 711: 710: 702: 701: 695: 689: 688: 683: 678: 674: 673: 663: 662: 659: 658: 647: 646: 644: 643: 638: 633: 628: 623: 617: 615: 611: 610: 608: 607: 602: 597: 592: 587: 582: 580:nuclear matrix 576: 574: 570: 569: 567: 566: 561: 556: 551: 545: 543: 539: 538: 528: 527: 524: 523: 520: 519: 511: 510: 485: 479: 478: 475: 474: 466: 465: 462: 461: 459: 458: 457:tail of embryo 454: 450: 446: 442: 438: 434: 430: 426: 422: 418: 415: 414: 403: 400: 399: 397: 396: 392: 391:gastric mucosa 388: 387:body of uterus 384: 380: 376: 372: 368: 364: 360: 356: 353: 352: 340: 339: 331: 320: 314: 313: 310:RNA expression 302: 301: 298: 297: 289: 285: 284: 276: 273: 268: 262: 261: 252: 245: 239: 235: 234: 229: 223: 222: 214: 213: 201: 200: 197: 196: 188: 184: 183: 175: 172: 167: 161: 160: 151: 144: 138: 134: 133: 126: 120: 119: 111: 110: 98: 97: 54: 50: 49: 41: 33: 32: 28: 27: 24: 23: 15: 13: 10: 9: 6: 4: 3: 2: 2520: 2509: 2506: 2504: 2501: 2500: 2498: 2488: 2484: 2483: 2478: 2477: 2472: 2469: 2465: 2462: 2460: 2457: 2456: 2452: 2445: 2441: 2436: 2431: 2427: 2423: 2419: 2414: 2410: 2406: 2401: 2396: 2391: 2386: 2382: 2378: 2375:(7): 3491–6. 2374: 2370: 2366: 2360: 2356: 2352: 2347: 2342: 2339:(6): 947–57. 2338: 2334: 2330: 2325: 2321: 2317: 2312: 2307: 2303: 2299: 2295: 2290: 2286: 2282: 2278: 2274: 2270: 2266: 2263:(6): 547–52. 2262: 2258: 2252: 2248: 2244: 2240: 2236: 2231: 2226: 2223:(3): 149–60. 2222: 2218: 2214: 2209: 2205: 2201: 2196: 2191: 2187: 2183: 2179: 2173: 2169: 2165: 2160: 2155: 2151: 2147: 2143: 2138: 2134: 2130: 2125: 2120: 2117:(3): 268–80. 2116: 2112: 2108: 2103: 2099: 2095: 2090: 2085: 2082:(2): 219–26. 2081: 2077: 2073: 2068: 2064: 2060: 2055: 2050: 2046: 2042: 2038: 2032: 2028: 2024: 2020: 2016: 2012: 2008: 2003: 1999: 1995: 1990: 1985: 1982:(4): 314–26. 1981: 1977: 1973: 1968: 1964: 1960: 1955: 1950: 1946: 1942: 1938: 1933: 1929: 1925: 1921: 1917: 1913: 1909: 1905: 1901: 1895: 1891: 1887: 1883: 1879: 1875: 1871: 1867: 1863: 1857: 1853: 1849: 1845: 1841: 1837: 1833: 1829: 1825: 1819: 1815: 1811: 1807: 1803: 1799: 1795: 1792:(2): 177–82. 1791: 1787: 1781: 1777: 1773: 1769: 1765: 1761: 1757: 1754:(1): 99–103. 1753: 1749: 1744: 1740: 1736: 1731: 1726: 1722: 1718: 1714: 1709: 1705: 1701: 1696: 1691: 1687: 1683: 1680:(5): 525–30. 1679: 1675: 1671: 1666: 1665: 1660: 1651: 1647: 1642: 1637: 1633: 1629: 1625: 1618: 1615: 1610: 1606: 1602: 1598: 1593: 1588: 1585:(3): 149–60. 1584: 1580: 1576: 1569: 1567: 1565: 1561: 1556: 1552: 1547: 1542: 1539:(6): 947–57. 1538: 1534: 1530: 1523: 1520: 1509: 1505: 1499: 1497: 1493: 1488: 1484: 1479: 1474: 1471:(4): 378–84. 1470: 1466: 1462: 1455: 1453: 1451: 1449: 1447: 1443: 1438: 1434: 1429: 1424: 1420: 1416: 1412: 1405: 1402: 1391: 1387: 1381: 1379: 1377: 1375: 1373: 1369: 1364: 1360: 1356: 1352: 1347: 1342: 1338: 1334: 1331:(3): 437–46. 1330: 1326: 1322: 1315: 1312: 1307: 1303: 1298: 1293: 1289: 1285: 1282:(5): 939–48. 1281: 1277: 1273: 1266: 1264: 1262: 1258: 1253: 1247: 1244: 1233: 1229: 1223: 1221: 1219: 1215: 1210: 1206: 1200: 1197: 1192: 1188: 1182: 1179: 1175: 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533: 529: 517: 512: 508: 501: 494: 489: 486: 484: 480: 472: 467: 456: 452: 448: 444: 440: 436: 432: 428: 424: 420: 419: 416: 412: 407: 404: 394: 390: 386: 382: 378: 374: 370: 366: 362: 358: 357: 354: 350: 345: 342: 341: 338: 336: 332: 330: 329: 325: 324: 321: 319: 315: 311: 307: 303: 295: 290: 286: 282: 277: 267: 263: 256: 249: 243: 236: 228: 224: 220: 215: 211: 206: 202: 194: 189: 185: 181: 176: 166: 162: 155: 148: 142: 135: 131: 125: 121: 117: 112: 108: 103: 99: 95: 91: 87: 83: 79: 75: 71: 67: 63: 59: 51: 46: 39: 34: 29: 25: 20: 2481: 2475: 2425: 2421: 2372: 2368: 2336: 2332: 2304:(3): 453–7. 2301: 2297: 2260: 2256: 2220: 2216: 2185: 2181: 2149: 2145: 2114: 2110: 2079: 2075: 2047:(3): 373–9. 2044: 2040: 2013:(1): 171–2. 2010: 2006: 1979: 1975: 1947:(3): 572–9. 1944: 1940: 1903: 1899: 1865: 1861: 1830:(4): 521–4. 1827: 1823: 1789: 1785: 1751: 1747: 1720: 1716: 1677: 1673: 1631: 1627: 1617: 1582: 1578: 1536: 1532: 1522: 1511:. Retrieved 1507: 1468: 1464: 1418: 1414: 1404: 1393:. Retrieved 1389: 1328: 1324: 1314: 1279: 1275: 1246: 1235:. Retrieved 1231: 1208: 1199: 1190: 1181: 1090: 1087:Interactions 1080: 1050: 1038: 1025:co-repressor 1021:co-repressor 1018: 1005:co-repressor 992: 991: 914: 892:NP_001007027 889: 863: 845:NM_001007026 838: 814: 795: 769: 750: 724: 705: 685: 680: 333: 326: 292:124,733,487 279:124,719,507 53:External IDs 1906:(1): 9–13. 1868:(1): 14–8. 1386:"ATN1 gene" 595:nucleoplasm 564:DNA binding 375:right ovary 31:Identifiers 2497:Categories 2464:atrophin-1 1513:2017-02-21 1395:2017-02-21 1237:2017-03-12 1176:, May 2017 1155:, May 2017 1131:References 1055:known as " 993:Atrophin-1 367:left ovary 337:(ortholog) 191:6,942,321 178:6,924,463 74:HomoloGene 917:NP_031907 896:NP_001931 866:NM_007881 841:NM_001940 671:Orthologs 600:cytoplasm 82:GeneCards 2444:10814707 2409:10737800 2355:10332026 2285:12861680 2247:20003277 2007:Genomics 1941:Genomics 1928:27241147 1890:19708585 1852:40759301 1704:16481466 1650:10814707 1609:20003277 1555:10332026 1487:21577324 1437:17150957 1363:11380927 1355:18953689 1346:11131516 1306:10973986 1172:– 1151:– 1093:interact 1077:dementia 1015:Function 965:Wikidata 650:Sources: 170:12p13.31 2377:Bibcode 2320:9949204 2277:9845282 2239:9647693 2204:9535906 2168:9361003 2133:9074930 2098:8965642 2063:8852663 2027:8786114 1998:8723724 1963:8325628 1920:8136840 1882:8136826 1844:7951323 1814:2590882 1806:7842016 1776:5850726 1768:7647802 1739:7485154 1730:1801383 1695:1410805 1601:9647693 1478:3093063 1297:2175251 1174:Ensembl 1153:Ensembl 997:protein 783:UniProt 738:Ensembl 677:Species 656:QuickGO 605:nucleus 312:pattern 38:Aliases 2473:Human 2470:(MeSH) 2442:  2407:  2397:  2353:  2318:  2283:  2275:  2245:  2237:  2202:  2166:  2131:  2096:  2061:  2025:  1996:  1961:  1926:  1918:  1888:  1880:  1850:  1842:  1812:  1804:  1774:  1766:  1737:  1727:  1702:  1692:  1648:  1607:  1599:  1553:  1485:  1475:  1435:  1361:  1353:  1343:  1304:  1294:  1120:, and 1100:BAIAP2 1095:with: 1075:, and 951:search 949:PubMed 816:O35126 797:P54259 693:Entrez 483:BioGPS 70:104725 62:607462 2400:16267 2281:S2CID 2243:S2CID 1924:S2CID 1886:S2CID 1848:S2CID 1810:S2CID 1772:S2CID 1605:S2CID 1359:S2CID 1112:MAGI2 1106:MAGI1 995:is a 726:13498 686:Mouse 681:Human 652:Amigo 335:Mouse 328:Human 275:Start 210:Mouse 174:Start 107:Human 2482:ATN1 2476:ATN1 2440:PMID 2405:PMID 2351:PMID 2316:PMID 2273:PMID 2235:PMID 2200:PMID 2164:PMID 2129:PMID 2094:PMID 2059:PMID 2023:PMID 1994:PMID 1959:PMID 1916:PMID 1878:PMID 1840:PMID 1802:PMID 1764:PMID 1735:PMID 1700:PMID 1646:PMID 1597:PMID 1551:PMID 1483:PMID 1433:PMID 1351:PMID 1302:PMID 1124:WWP2 1118:RERE 1001:gene 707:1822 318:Bgee 266:Band 227:Chr. 165:Band 124:Chr. 86:ATN1 78:1461 58:OMIM 45:ATN1 22:ATN1 2430:doi 2395:PMC 2385:doi 2341:doi 2306:doi 2265:doi 2225:doi 2190:doi 2186:273 2154:doi 2150:272 2119:doi 2084:doi 2049:doi 2015:doi 1984:doi 1949:doi 1908:doi 1870:doi 1832:doi 1794:doi 1756:doi 1725:PMC 1690:PMC 1682:doi 1636:doi 1587:doi 1541:doi 1473:PMC 1423:doi 1419:282 1341:PMC 1333:doi 1292:PMC 1284:doi 1280:150 449:lip 288:End 187:End 90:OMA 66:MGI 2499:: 2438:. 2424:. 2420:. 2403:. 2393:. 2383:. 2373:97 2371:. 2367:. 2349:. 2335:. 2331:. 2314:. 2300:. 2296:. 2279:. 2271:. 2261:96 2259:. 2241:. 2233:. 2221:11 2219:. 2215:. 2198:. 2184:. 2180:. 2162:. 2148:. 2144:. 2127:. 2113:. 2109:. 2092:. 2080:36 2078:. 2074:. 2057:. 2043:. 2039:. 2021:. 2011:32 2009:. 1992:. 1978:. 1974:. 1957:. 1945:16 1943:. 1939:. 1922:. 1914:. 1902:. 1884:. 1876:. 1864:. 1846:. 1838:. 1826:. 1808:. 1800:. 1788:. 1770:. 1762:. 1752:10 1750:. 1733:. 1721:57 1719:. 1715:. 1698:. 1688:. 1678:20 1676:. 1672:. 1644:. 1630:. 1626:. 1603:. 1595:. 1583:11 1581:. 1577:. 1563:^ 1549:. 1535:. 1531:. 1506:. 1495:^ 1481:. 1467:. 1463:. 1445:^ 1431:. 1417:. 1413:. 1388:. 1371:^ 1357:. 1349:. 1339:. 1329:66 1327:. 1323:. 1300:. 1290:. 1278:. 1274:. 1260:^ 1230:. 1217:^ 1207:. 1189:. 1160:^ 1139:^ 1071:, 1067:, 1031:. 1011:. 654:/ 294:bp 281:bp 193:bp 180:bp 88:; 84:: 80:; 76:: 72:; 68:: 64:; 60:: 2489:. 2446:. 2432:: 2426:9 2411:. 2387:: 2379:: 2357:. 2343:: 2337:8 2322:. 2308:: 2302:8 2287:. 2267:: 2249:. 2227:: 2206:. 2192:: 2170:. 2156:: 2135:. 2121:: 2115:7 2100:. 2086:: 2065:. 2051:: 2045:5 2029:. 2017:: 2000:. 1986:: 1980:6 1965:. 1951:: 1930:. 1910:: 1904:6 1892:. 1872:: 1866:6 1854:. 1834:: 1828:7 1816:. 1796:: 1790:8 1778:. 1758:: 1741:. 1706:. 1684:: 1652:. 1638:: 1632:9 1611:. 1589:: 1557:. 1543:: 1537:8 1516:. 1489:. 1469:4 1439:. 1425:: 1398:. 1365:. 1335:: 1308:. 1286:: 1254:. 1240:. 1211:. 1193:. 1126:. 1114:, 1108:, 1102:, 212:) 109:) 92::

Index

Aliases
ATN1
OMIM
607462
MGI
104725
HomoloGene
1461
GeneCards
ATN1
OMA
ATN1 - orthologs
Human
Chromosome 12 (human)
Chr.
Chromosome 12 (human)
Chromosome 12 (human)
Genomic location for ATN1
Genomic location for ATN1
Band
bp
bp
Mouse
Chromosome 6 (mouse)
Chr.
Chromosome 6 (mouse)
Genomic location for ATN1
Genomic location for ATN1
Band
bp

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