Knowledge

Atrophin 1

Source πŸ“

253: 230: 152: 127: 504: 511: 518: 259: 158: 1014:. 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 2373:
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".
2305:"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" 1059:(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. 1055:
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".
2340:"Dentatorubral-pallidoluysian atrophy protein interacts through a proline-rich region near polyglutamine with the SH3 domain of an insulin receptor tyrosine kinase substrate" 1540:"Dentatorubral-pallidoluysian atrophy protein interacts through a proline-rich region near polyglutamine with the SH3 domain of an insulin receptor tyrosine kinase substrate" 1757:
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".
736: 717: 88: 1283:"Atrophin-1, the dentato-rubral and pallido-luysian atrophy gene product, interacts with ETO/MTG8 in the nuclear matrix and represses transcription" 2189:"Caspase cleavage of gene products associated with triplet expansion disorders generates truncated fragments containing the polyglutamine tract" 1724:"Molecular cloning of a full-length cDNA for dentatorubral-pallidoluysian atrophy and regional expressions of the expanded alleles in the CNS" 1215: 1197: 951: 2485: 944: 1262: 1030:
The function of Atrophin-1 has not been defined yet. It is widely hypothesized that Atrophin-1 functions as a transcriptional
2513: 1180: 1067: 2491: 2429:"Protein binding of a DRPLA family through arginine-glutamic acid dipeptide repeats is enhanced by extended polyglutamine" 1635:"Protein binding of a DRPLA family through arginine-glutamic acid dipeptide repeats is enhanced by extended polyglutamine" 2518: 1159: 2222:
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).
252: 1184: 1163: 229: 2118:"Large-scale sequencing in human chromosome 12p13: experimental and computational gene structure determination" 1281:
Wood JD, Nucifora FC, Duan K, Zhang C, Wang J, Kim Y, Schilling G, Sacchi N, Liu JM, Ross CA (September 2000).
781: 1063: 151: 126: 762: 68: 2469: 1103: 1018:. Atrophin-1 can be found in the nuclear and cytoplasmic compartments of neurons. It is expressed in 265: 164: 1948:"Novel triplet repeat containing genes in human brain: cloning, expression, and length polymorphisms" 258: 157: 55: 2478: 1983:"A gene-rich cluster between the CD4 and triosephosphate isomerase genes at human chromosome 12p13" 902: 855: 76: 2224:"Atrophin-1, the DRPLA gene product, interacts with two families of WW domain-containing proteins" 2081:
Margolis RL, Li SH, Young WS, Wagster MV, Stine OC, Kidwai AS, Ashworth RG, Ross CA (March 1996).
1586:"Atrophin-1, the DRPLA gene product, interacts with two families of WW domain-containing proteins" 1070:" or "dentatorubropallidoluysian atrophy". Dentatorubral-pallidoluysian atrophy (DRPLA) is a rare 2427:
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).
927: 906: 876: 851: 2153:"Dentatorubral pallidoluysian atrophy (DRPLA) protein is cleaved by caspase-3 during apoptosis" 1094:
adult-onset variants of DRPLA, which show differing degrees of severity of specific symptoms.
1056: 140: 2048:"A unique origin and multistep process for the generation of expanded DRPLA triplet repeats" 1981:
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).
2291: 2253: 1934: 1896: 1858: 1820: 1782: 1740: 1723: 1705: 1680: 1615: 1488: 1471: 1369: 1307: 1282: 1090:. The disorder is related to the expansion of a trinucleotide repeat within this gene. 1079: 100: 2474: 651: 646: 641: 636: 631: 615: 610: 605: 600: 595: 590: 574: 569: 564: 559: 2450: 2415: 2410: 2375: 2361: 2326: 2283: 2245: 2210: 2174: 2139: 2104: 2099: 2082: 2069: 2033: 2004: 1969: 1926: 1888: 1850: 1812: 1774: 1745: 1710: 1681:"Histone deacetylase-associating Atrophin proteins are nuclear receptor corepressors" 1656: 1607: 1561: 1493: 1443: 1361: 1312: 1075: 1071: 48: 2295: 2257: 1938: 1900: 1862: 1619: 1373: 2440: 2405: 2395: 2351: 2316: 2275: 2235: 2200: 2164: 2129: 2094: 2059: 2025: 1994: 1959: 1918: 1880: 1842: 1824: 1804: 1786: 1766: 1735: 1700: 1692: 1646: 1597: 1551: 1483: 1433: 1396: 1351: 1343: 1302: 1294: 345: 276: 220: 175: 80: 1514: 1083: 320: 104: 2376:"Shotgun sequencing of the human transcriptome with ORF expressed sequence tags" 1472:"Pathological accumulation of atrophin-1 in dentatorubralpallidoluysian atrophy" 1220:
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).
2029: 1964: 1947: 1714: 1660: 1651: 1634: 1602: 1585: 1565: 1497: 1447: 1438: 1421: 1365: 1316: 1035: 1031: 1015: 510: 338: 117: 2356: 2339: 2330: 2321: 2304: 2287: 2279: 2249: 2214: 2178: 2143: 2108: 2073: 2064: 2047: 2037: 2008: 1973: 1930: 1892: 1854: 1816: 1778: 1749: 1611: 1556: 1539: 1298: 991: 986: 517: 1238: 826: 807: 1696: 1332:"Atrophins' emerging roles in development and neurodegenerative disease" 2372: 2134: 2117: 1999: 1982: 1846: 1808: 237: 134: 84: 1884: 1770: 2083:"DRPLA gene (atrophin-1) sequence and mRNA expression in human brain" 1946:
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).
2044: 1869: 72: 2185: 2015: 1110: 959: 703: 526: 2337: 1537: 1239:"ATN1 atrophin 1 [Homo sapiens (human)] - Gene - NCBI" 1679:
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
2264: 1831: 328: 2221: 2115: 1756: 1583: 2080: 1678: 1280: 493: 1980: 1419: 59:, B37, D12S755E, DRPLA, HRS, NOD, atrophin 1, CHEDDA 448:
dentate gyrus of hippocampal formation granule cell
1176: 1174: 1172: 1155: 1153: 1151: 275: 174: 2505: 1062:Mutations in ATN1 are associated with a form of 1169: 1148: 1579: 1577: 1575: 1465: 1463: 1461: 1459: 1457: 1181:GRCm38: Ensembl release 89: ENSMUSG00000004263 1515:"Dentatorubral-Pallidoluysian Atrophy, DRPLA" 1233: 1231: 1229: 1626: 1531: 1469: 1329: 1572: 1454: 1276: 1274: 1272: 1160:GRCh38: Ensembl release 89: ENSG00000111676 1226: 642:regulation of transcription, DNA-templated 2477:at the U.S. National Library of Medicine 2444: 2409: 2399: 2355: 2320: 2239: 2204: 2168: 2133: 2098: 2063: 1998: 1963: 1739: 1704: 1650: 1601: 1555: 1487: 1437: 1355: 1306: 2087:Brain Research. Molecular Brain Research 1269: 1045: 14: 2506: 2470:GeneReviews/NCBI/NIH/UW entry on DRPLA 1422:"Functional architecture of atrophins" 1010:that in humans is encoded by the ATN1 1391: 1389: 1387: 1385: 1383: 1330:Shen Y, Peterson AS (February 2009). 1255: 280: 241: 236: 179: 138: 133: 2228:Molecular and Cellular Neurosciences 1590:Molecular and Cellular Neurosciences 1336:Cellular and Molecular Life Sciences 1068:dentatorubral-pallidoluysian atrophy 2193:The Journal of Biological Chemistry 2157:The Journal of Biological Chemistry 1426:The Journal of Biological Chemistry 24: 1728:American Journal of Human Genetics 1671: 1380: 637:central nervous system development 565:transcription corepressor activity 25: 2530: 2463: 1470:Suzuki Y, Yazawa I (April 2011). 516: 509: 502: 264: 257: 251: 228: 163: 156: 150: 125: 1413: 1097: 596:perinuclear region of cytoplasm 570:protein domain specific binding 1519:themedicalbiochemistrypage.org 1323: 1263:"Entrez Gene: ATN1 atrophin 1" 1208: 1190: 527:More reference expression data 482:More reference expression data 370:right hemisphere of cerebellum 13: 1: 1141: 1064:trinucleotide repeat disorder 249: 148: 2514:Genes on human chromosome 12 2100:10.1016/0169-328X(95)00241-J 652:transcription, DNA-templated 7: 1287:The Journal of Cell Biology 1025: 390:right lobe of thyroid gland 10: 2535: 2519:Transcription coregulators 2496:gene details page in the 1074:disorder characterized by 394:left lobe of thyroid gland 1348:10.1007/s00018-008-8403-9 1216:"Mouse PubMed Reference:" 1198:"Human PubMed Reference:" 1053:gain-of-function mutation 990: 985: 981: 974: 958: 952:Chr 6: 124.72 – 124.73 Mb 939: 924: 920: 899: 895: 888: 873: 869: 848: 844: 837: 824: 820: 805: 801: 792: 779: 775: 760: 756: 747: 734: 730: 715: 711: 702: 687: 680: 676: 660: 545: 541: 524: 501: 492: 479: 428: 419: 366: 357: 327: 319: 315: 298: 285: 248: 227: 218: 214: 197: 184: 147: 124: 115: 111: 66: 63: 53: 46: 41: 37: 32: 2479:Medical Subject Headings 2433:Human Molecular Genetics 2344:Human Molecular Genetics 2309:Human Molecular Genetics 2170:10.1074/jbc.272.46.29238 2052:Human Molecular Genetics 1639:Human Molecular Genetics 1544:Human Molecular Genetics 632:neuron apoptotic process 2206:10.1074/jbc.273.15.9158 1685:Genes & Development 1401:Genetics Home Reference 1102:ATN1 has been shown to 27:Protein found in humans 2401:10.1073/pnas.97.7.3491 2241:10.1006/mcne.1998.0677 2030:10.1006/geno.1996.0100 1965:10.1006/geno.1993.1232 1603:10.1006/mcne.1998.0677 1439:10.1074/jbc.M610274200 945:Chr 12: 6.92 – 6.94 Mb 440:superior frontal gyrus 432:neural layer of retina 2280:10.1007/s004010050933 2268:Acta Neuropathologica 1299:10.1083/jcb.150.5.939 1057:nuclear export signal 1046:Clinical significance 436:primary visual cortex 141:Chromosome 12 (human) 2490:genome location and 2446:10.1093/hmg/9.9.1433 1652:10.1093/hmg/9.9.1433 1243:www.ncbi.nlm.nih.gov 1040:DNA-binding proteins 1034:. A transcriptional 282:6 F2|6 59.17 cM 243:Chromosome 6 (mouse) 2498:UCSC Genome Browser 2392:2000PNAS...97.3491D 2357:10.1093/hmg/8.6.947 2322:10.1093/hmg/8.3.453 2065:10.1093/hmg/5.3.373 1697:10.1101/gad.1393506 1557:10.1093/hmg/8.6.947 406:canal of the cervix 2135:10.1101/gr.7.3.268 2000:10.1101/gr.6.4.314 1847:10.1038/ng0894-521 1809:10.1038/ng1094-177 1080:myoclonic epilepsy 782:ENSMUSG00000004263 625:Biological process 584:Cellular component 553:Molecular function 382:right uterine tube 374:anterior pituitary 1885:10.1038/ng0194-14 1771:10.1038/ng0595-99 1076:cerebellar ataxia 1072:neurodegenerative 1001: 1000: 997: 996: 970: 969: 935: 934: 914: 913: 884: 883: 863: 862: 833: 832: 814: 813: 788: 787: 769: 768: 743: 742: 724: 723: 672: 671: 537: 536: 533: 532: 488: 487: 475: 474: 452:cerebellar cortex 413: 412: 311: 310: 210: 209: 16:(Redirected from 2526: 2458: 2448: 2423: 2413: 2403: 2369: 2359: 2334: 2324: 2299: 2261: 2243: 2218: 2208: 2182: 2172: 2163:(46): 29238–42. 2147: 2137: 2112: 2102: 2077: 2067: 2041: 2012: 2002: 1977: 1967: 1942: 1923:10.1038/ng0194-9 1904: 1866: 1828: 1790: 1753: 1743: 1718: 1708: 1665: 1664: 1654: 1630: 1624: 1623: 1605: 1581: 1570: 1569: 1559: 1535: 1529: 1528: 1526: 1525: 1511: 1502: 1501: 1491: 1467: 1452: 1451: 1441: 1417: 1411: 1410: 1408: 1407: 1393: 1378: 1377: 1359: 1327: 1321: 1320: 1310: 1278: 1267: 1266: 1259: 1253: 1252: 1250: 1249: 1235: 1224: 1223: 1212: 1206: 1205: 1194: 1188: 1178: 1167: 1157: 983: 982: 954: 947: 930: 918: 917: 909: 893: 892: 889:RefSeq (protein) 879: 867: 866: 858: 842: 841: 818: 817: 799: 798: 773: 772: 754: 753: 728: 727: 709: 708: 678: 677: 543: 542: 529: 520: 513: 506: 499: 498: 484: 464:ventricular zone 444:genital tubercle 424: 422:Top expressed in 417: 416: 362: 360:Top expressed in 355: 354: 334: 333: 317: 316: 307: 294: 283: 268: 261: 255: 244: 232: 216: 215: 206: 193: 182: 167: 160: 154: 143: 129: 113: 112: 107: 105:ATN1 - orthologs 58: 51: 30: 29: 21: 2534: 2533: 2529: 2528: 2527: 2525: 2524: 2523: 2504: 2503: 2466: 2461: 2199:(15): 9158–67. 2122:Genome Research 1987:Genome Research 1911:Nature Genetics 1873:Nature Genetics 1835:Nature Genetics 1797:Nature Genetics 1759:Nature Genetics 1674: 1672:Further reading 1669: 1668: 1631: 1627: 1582: 1573: 1536: 1532: 1523: 1521: 1513: 1512: 1505: 1468: 1455: 1418: 1414: 1405: 1403: 1395: 1394: 1381: 1328: 1324: 1279: 1270: 1261: 1260: 1256: 1247: 1245: 1237: 1236: 1227: 1214: 1213: 1209: 1196: 1195: 1191: 1179: 1170: 1158: 1149: 1144: 1100: 1084:choreoathetosis 1048: 1028: 992:View/Edit Mouse 987:View/Edit Human 950: 943: 940:Location (UCSC) 926: 905: 901: 875: 854: 850: 763:ENSG00000111676 656: 620: 579: 560:protein binding 525: 515: 514: 508: 507: 480: 471: 466: 462: 458: 456:muscle of thigh 454: 450: 446: 442: 438: 434: 420: 409: 404: 400: 396: 392: 388: 384: 380: 376: 372: 358: 302: 289: 281: 271: 270: 269: 262: 242: 219:Gene location ( 201: 188: 180: 170: 169: 168: 161: 139: 116:Gene location ( 67: 54: 47: 28: 23: 22: 15: 12: 11: 5: 2532: 2522: 2521: 2516: 2502: 2501: 2482: 2472: 2465: 2464:External links 2462: 2460: 2459: 2439:(9): 1433–42. 2424: 2370: 2335: 2300: 2262: 2219: 2183: 2148: 2113: 2078: 2042: 2013: 1978: 1943: 1905: 1867: 1829: 1791: 1754: 1734:(5): 1050–60. 1719: 1675: 1673: 1670: 1667: 1666: 1645:(9): 1433–42. 1625: 1571: 1530: 1503: 1453: 1432:(7): 5037–44. 1412: 1379: 1322: 1268: 1254: 1225: 1207: 1189: 1168: 1146: 1145: 1143: 1140: 1139: 1138: 1132: 1126: 1120: 1114: 1099: 1096: 1047: 1044: 1027: 1024: 1020:nervous tissue 999: 998: 995: 994: 989: 979: 978: 972: 971: 968: 967: 965: 963: 956: 955: 948: 941: 937: 936: 933: 932: 922: 921: 915: 912: 911: 897: 896: 890: 886: 885: 882: 881: 871: 870: 864: 861: 860: 846: 845: 839: 835: 834: 831: 830: 822: 821: 815: 812: 811: 803: 802: 796: 790: 789: 786: 785: 777: 776: 770: 767: 766: 758: 757: 751: 745: 744: 741: 740: 732: 731: 725: 722: 721: 713: 712: 706: 700: 699: 694: 689: 685: 684: 674: 673: 670: 669: 658: 657: 655: 654: 649: 644: 639: 634: 628: 626: 622: 621: 619: 618: 613: 608: 603: 598: 593: 591:nuclear matrix 587: 585: 581: 580: 578: 577: 572: 567: 562: 556: 554: 550: 549: 539: 538: 535: 534: 531: 530: 522: 521: 496: 490: 489: 486: 485: 477: 476: 473: 472: 470: 469: 468:tail of embryo 465: 461: 457: 453: 449: 445: 441: 437: 433: 429: 426: 425: 414: 411: 410: 408: 407: 403: 402:gastric mucosa 399: 398:body of uterus 395: 391: 387: 383: 379: 375: 371: 367: 364: 363: 351: 350: 342: 331: 325: 324: 321:RNA expression 313: 312: 309: 308: 300: 296: 295: 287: 284: 279: 273: 272: 263: 256: 250: 246: 245: 240: 234: 233: 225: 224: 212: 211: 208: 207: 199: 195: 194: 186: 183: 178: 172: 171: 162: 155: 149: 145: 144: 137: 131: 130: 122: 121: 109: 108: 65: 61: 60: 52: 44: 43: 39: 38: 35: 34: 26: 9: 6: 4: 3: 2: 2531: 2520: 2517: 2515: 2512: 2511: 2509: 2499: 2495: 2494: 2489: 2488: 2483: 2480: 2476: 2473: 2471: 2468: 2467: 2456: 2452: 2447: 2442: 2438: 2434: 2430: 2425: 2421: 2417: 2412: 2407: 2402: 2397: 2393: 2389: 2386:(7): 3491–6. 2385: 2381: 2377: 2371: 2367: 2363: 2358: 2353: 2350:(6): 947–57. 2349: 2345: 2341: 2336: 2332: 2328: 2323: 2318: 2314: 2310: 2306: 2301: 2297: 2293: 2289: 2285: 2281: 2277: 2274:(6): 547–52. 2273: 2269: 2263: 2259: 2255: 2251: 2247: 2242: 2237: 2234:(3): 149–60. 2233: 2229: 2225: 2220: 2216: 2212: 2207: 2202: 2198: 2194: 2190: 2184: 2180: 2176: 2171: 2166: 2162: 2158: 2154: 2149: 2145: 2141: 2136: 2131: 2128:(3): 268–80. 2127: 2123: 2119: 2114: 2110: 2106: 2101: 2096: 2093:(2): 219–26. 2092: 2088: 2084: 2079: 2075: 2071: 2066: 2061: 2057: 2053: 2049: 2043: 2039: 2035: 2031: 2027: 2023: 2019: 2014: 2010: 2006: 2001: 1996: 1993:(4): 314–26. 1992: 1988: 1984: 1979: 1975: 1971: 1966: 1961: 1957: 1953: 1949: 1944: 1940: 1936: 1932: 1928: 1924: 1920: 1916: 1912: 1906: 1902: 1898: 1894: 1890: 1886: 1882: 1878: 1874: 1868: 1864: 1860: 1856: 1852: 1848: 1844: 1840: 1836: 1830: 1826: 1822: 1818: 1814: 1810: 1806: 1803:(2): 177–82. 1802: 1798: 1792: 1788: 1784: 1780: 1776: 1772: 1768: 1765:(1): 99–103. 1764: 1760: 1755: 1751: 1747: 1742: 1737: 1733: 1729: 1725: 1720: 1716: 1712: 1707: 1702: 1698: 1694: 1691:(5): 525–30. 1690: 1686: 1682: 1677: 1676: 1662: 1658: 1653: 1648: 1644: 1640: 1636: 1629: 1621: 1617: 1613: 1609: 1604: 1599: 1596:(3): 149–60. 1595: 1591: 1587: 1580: 1578: 1576: 1567: 1563: 1558: 1553: 1550:(6): 947–57. 1549: 1545: 1541: 1534: 1520: 1516: 1510: 1508: 1499: 1495: 1490: 1485: 1482:(4): 378–84. 1481: 1477: 1473: 1466: 1464: 1462: 1460: 1458: 1449: 1445: 1440: 1435: 1431: 1427: 1423: 1416: 1402: 1398: 1392: 1390: 1388: 1386: 1384: 1375: 1371: 1367: 1363: 1358: 1353: 1349: 1345: 1342:(3): 437–46. 1341: 1337: 1333: 1326: 1318: 1314: 1309: 1304: 1300: 1296: 1293:(5): 939–48. 1292: 1288: 1284: 1277: 1275: 1273: 1264: 1258: 1244: 1240: 1234: 1232: 1230: 1221: 1217: 1211: 1203: 1199: 1193: 1186: 1182: 1177: 1175: 1173: 1165: 1161: 1156: 1154: 1152: 1147: 1136: 1133: 1130: 1127: 1124: 1121: 1118: 1115: 1112: 1109: 1108: 1107: 1105: 1095: 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Retrieved 1518: 1479: 1475: 1429: 1425: 1415: 1404:. Retrieved 1400: 1339: 1335: 1325: 1290: 1286: 1257: 1246:. Retrieved 1242: 1219: 1210: 1201: 1192: 1101: 1098:Interactions 1091: 1061: 1049: 1036:co-repressor 1032:co-repressor 1029: 1016:co-repressor 1003: 1002: 925: 903:NP_001007027 900: 874: 856:NM_001007026 849: 825: 806: 780: 761: 735: 716: 696: 691: 344: 337: 303:124,733,487 290:124,719,507 64:External IDs 1917:(1): 9–13. 1879:(1): 14–8. 1397:"ATN1 gene" 606:nucleoplasm 575:DNA binding 386:right ovary 42:Identifiers 2508:Categories 2475:atrophin-1 1524:2017-02-21 1406:2017-02-21 1248:2017-03-12 1187:, May 2017 1166:, May 2017 1142:References 1066:known as " 1004:Atrophin-1 378:left ovary 348:(ortholog) 202:6,942,321 189:6,924,463 85:HomoloGene 928:NP_031907 907:NP_001931 877:NM_007881 852:NM_001940 682:Orthologs 611:cytoplasm 93:GeneCards 2455:10814707 2420:10737800 2366:10332026 2296:12861680 2258:20003277 2018:Genomics 1952:Genomics 1939:27241147 1901:19708585 1863:40759301 1715:16481466 1661:10814707 1620:20003277 1566:10332026 1498:21577324 1448:17150957 1374:11380927 1366:18953689 1357:11131516 1317:10973986 1183:– 1162:– 1104:interact 1088:dementia 1026:Function 976:Wikidata 661:Sources: 181:12p13.31 2388:Bibcode 2331:9949204 2288:9845282 2250:9647693 2215:9535906 2179:9361003 2144:9074930 2109:8965642 2074:8852663 2038:8786114 2009:8723724 1974:8325628 1931:8136840 1893:8136826 1855:7951323 1825:2590882 1817:7842016 1787:5850726 1779:7647802 1750:7485154 1741:1801383 1706:1410805 1612:9647693 1489:3093063 1308:2175251 1185:Ensembl 1164:Ensembl 1008:protein 794:UniProt 749:Ensembl 688:Species 667:QuickGO 616:nucleus 323:pattern 49:Aliases 2484:Human 2481:(MeSH) 2453:  2418:  2408:  2364:  2329:  2294:  2286:  2256:  2248:  2213:  2177:  2142:  2107:  2072:  2036:  2007:  1972:  1937:  1929:  1899:  1891:  1861:  1853:  1823:  1815:  1785:  1777:  1748:  1738:  1713:  1703:  1659:  1618:  1610:  1564:  1496:  1486:  1446:  1372:  1364:  1354:  1315:  1305:  1131:, and 1111:BAIAP2 1106:with: 1086:, and 962:search 960:PubMed 827:O35126 808:P54259 704:Entrez 494:BioGPS 81:104725 73:607462 2411:16267 2292:S2CID 2254:S2CID 1935:S2CID 1897:S2CID 1859:S2CID 1821:S2CID 1783:S2CID 1616:S2CID 1370:S2CID 1123:MAGI2 1117:MAGI1 1006:is a 737:13498 697:Mouse 692:Human 663:Amigo 346:Mouse 339:Human 286:Start 221:Mouse 185:Start 118:Human 2493:ATN1 2487:ATN1 2451:PMID 2416:PMID 2362:PMID 2327:PMID 2284:PMID 2246:PMID 2211:PMID 2175:PMID 2140:PMID 2105:PMID 2070:PMID 2034:PMID 2005:PMID 1970:PMID 1927:PMID 1889:PMID 1851:PMID 1813:PMID 1775:PMID 1746:PMID 1711:PMID 1657:PMID 1608:PMID 1562:PMID 1494:PMID 1444:PMID 1362:PMID 1313:PMID 1135:WWP2 1129:RERE 1012:gene 718:1822 329:Bgee 277:Band 238:Chr. 176:Band 135:Chr. 97:ATN1 89:1461 69:OMIM 56:ATN1 33:ATN1 18:ATN1 2441:doi 2406:PMC 2396:doi 2352:doi 2317:doi 2276:doi 2236:doi 2201:doi 2197:273 2165:doi 2161:272 2130:doi 2095:doi 2060:doi 2026:doi 1995:doi 1960:doi 1919:doi 1881:doi 1843:doi 1805:doi 1767:doi 1736:PMC 1701:PMC 1693:doi 1647:doi 1598:doi 1552:doi 1484:PMC 1434:doi 1430:282 1352:PMC 1344:doi 1303:PMC 1295:doi 1291:150 460:lip 299:End 198:End 101:OMA 77:MGI 2510:: 2449:. 2435:. 2431:. 2414:. 2404:. 2394:. 2384:97 2382:. 2378:. 2360:. 2346:. 2342:. 2325:. 2311:. 2307:. 2290:. 2282:. 2272:96 2270:. 2252:. 2244:. 2232:11 2230:. 2226:. 2209:. 2195:. 2191:. 2173:. 2159:. 2155:. 2138:. 2124:. 2120:. 2103:. 2091:36 2089:. 2085:. 2068:. 2054:. 2050:. 2032:. 2022:32 2020:. 2003:. 1989:. 1985:. 1968:. 1956:16 1954:. 1950:. 1933:. 1925:. 1913:. 1895:. 1887:. 1875:. 1857:. 1849:. 1837:. 1819:. 1811:. 1799:. 1781:. 1773:. 1763:10 1761:. 1744:. 1732:57 1730:. 1726:. 1709:. 1699:. 1689:20 1687:. 1683:. 1655:. 1641:. 1637:. 1614:. 1606:. 1594:11 1592:. 1588:. 1574:^ 1560:. 1546:. 1542:. 1517:. 1506:^ 1492:. 1478:. 1474:. 1456:^ 1442:. 1428:. 1424:. 1399:. 1382:^ 1368:. 1360:. 1350:. 1340:66 1338:. 1334:. 1311:. 1301:. 1289:. 1285:. 1271:^ 1241:. 1228:^ 1218:. 1200:. 1171:^ 1150:^ 1082:, 1078:, 1042:. 1022:. 665:/ 305:bp 292:bp 204:bp 191:bp 99:; 95:: 91:; 87:: 83:; 79:: 75:; 71:: 2500:. 2457:. 2443:: 2437:9 2422:. 2398:: 2390:: 2368:. 2354:: 2348:8 2333:. 2319:: 2313:8 2298:. 2278:: 2260:. 2238:: 2217:. 2203:: 2181:. 2167:: 2146:. 2132:: 2126:7 2111:. 2097:: 2076:. 2062:: 2056:5 2040:. 2028:: 2011:. 1997:: 1991:6 1976:. 1962:: 1941:. 1921:: 1915:6 1903:. 1883:: 1877:6 1865:. 1845:: 1839:7 1827:. 1807:: 1801:8 1789:. 1769:: 1752:. 1717:. 1695:: 1663:. 1649:: 1643:9 1622:. 1600:: 1568:. 1554:: 1548:8 1527:. 1500:. 1480:4 1450:. 1436:: 1409:. 1376:. 1346:: 1319:. 1297:: 1265:. 1251:. 1222:. 1204:. 1137:. 1125:, 1119:, 1113:, 223:) 120:) 103:: 20:)

Index

ATN1
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

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