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ZFPM2

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244: 221: 2445: 118: 143: 495: 250: 149: 1186:. That is, the ZFPM2 protein appears able to interact directly with and thereby either enhance or repress the ability of GATA transcription factors to stimulate the expression of their target genes; the direction of ZFPM2's actions depends on the contexts of the 1715:
Brady PD, Van Houdt J, Callewaert B, Deprest J, Devriendt K, Vermeesch JR (2014). "Exome sequencing identifies ZFPM2 as a cause of familial isolated congenital diaphragmatic hernia and possibly cardiovascular malformations".
1370:, to stimulate the expression of their target genes. Interactions with the NuRD complex or a CTBP can cause ZFPM2 to inhibit the ability of GATA3-6 proteins to stimulate the expression of their target genes. 2495:
Finelli P, Pincelli AI, Russo S, et al. (2007). "Disruption of friend of GATA 2 gene (FOG-2) by a de novo t(8;10) chromosomal translocation is associated with heart defects and gonadal dysgenesis".
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Both the human and mouse ZFPM2 proteins consists of 1151 amino acids and are expressed in various tissues. The human protein is expressed at relatively high levels in the adult ovary and uterine
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family to modify their ability to stimulate the expression of their target genes. For example, it has been shown to bind directly with the N-terminal zinc finger of the
257: 156: 2535:"Candidate genes for congenital diaphragmatic hernia from animal models: sequencing of FOG2 and PDGFRalpha reveals rare variants in diaphragmatic hernia patients" 1354:
ZFPM2 regulates the expression of certain GATA target genes by up-regulating or down-regulating the ability of the GATA transcription factors, primarily
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Pu T, Liu Y, Xu R, Li F, Chen S, Sun K (February 2018). "Identification of ZFPM2 mutations in sporadic conotruncal heart defect patients".
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Cantor AB, Orkin SH (February 2005). "Coregulation of GATA factors by the Friend of GATA (FOG) family of multitype zinc finger proteins".
243: 1412: 1052: 1346:. that act to promote the ability of ZFPM2 to inhibit the ability of GATA proteins to stimulate the expression of their target genes. 1059: 220: 1698: 1546: 1525: 1458: 1226: 2250:
Pizzuti A, Sarkozy A, Newton AL, et al. (2004). "Mutations of ZFPM2/FOG2 gene in sporadic cases of tetralogy of Fallot".
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to humans. The human gene is located on the long or "q" arm of chromosome 8 at position 23.1 (i.e. 8q23.1) and consists of 9
1542: 142: 117: 2289:"FOG-2 competes with GATA-4 for transcriptional coactivator p300 and represses hypertrophic responses in cardiac myocytes" 1408: 1521: 1489: 1443:. These cases likely reflect the role of ZFPM2 in promoting GATA4's function in the embryonic development of the heart. 59: 256: 155: 1149: 1500:
of the ZFPM2 protein and consequential reduced regulation of GATA4 in promoting normal development of the gonads.
249: 148: 2121:"Proper coronary vascular development and heart morphogenesis depend on interaction of GATA-4 with FOG cofactors" 1754:
Brauner R, Picard-Dieval F, Lottmann H, Rouget S, Bignon-Topalovic J, Bashamboo A, McElreavey K (November 2016).
1404: 1309: 1183: 2217:"FOG-2 and GATA-4 Are coexpressed in the mouse ovary and can modulate mullerian-inhibiting substance expression" 1265:
is embryonic lethal in mice, with mice dying at embryonic day 12.5-15.5 due to congenital cardiac defects (thin
2454:"A protein-protein interaction network for human inherited ataxias and disorders of Purkinje cell degeneration" 1388: 873: 67: 2324:"The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC)" 1416: 1222: 854: 2444: 2078:"Transcriptional cofactors of the FOG family interact with GATA proteins by means of multiple zinc fingers" 2022:
Kardon G, Ackerman KG, McCulley DJ, Shen Y, Wynn J, Shang L, Bogenschutz E, Sun X, Chung WK (August 2017).
1656:"hFOG-2, a novel zinc finger protein, binds the co-repressor mCtBP2 and modulates GATA-mediated activation" 1466: 1270: 1175: 1756:"Familial forms of disorders of sex development may be common if infertility is considered a comorbidity" 1210: 1153: 1334:(i.e. nucleosome remodeling and histone deacetylase complex or NuRD complex) and other of which binds 2175: 1608: 1316: 131: 46: 1493: 1432: 1392: 1274: 1230: 1187: 1035: 1010: 1006: 976: 951: 947: 2521: 2483: 2275: 1963: 1497: 1470: 1396: 91: 2164:"Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences" 1031: 1002: 972: 943: 1461:. This development disorder may be the underlying cause for the development of congenital lung 2556: 2513: 2475: 2433: 2388: 2353: 2310: 2267: 2238: 2203: 2150: 2107: 2053: 2004: 1955: 1917: 1859: 1787: 1733: 1677: 1636: 1400: 1331: 1266: 39: 1809:"ZFPM2 zinc finger protein, FOG family member 2 [Homo sapiens (Human)] – Gene – NCBI" 1297:
while the mouse protein is expressed at relatively high levels in the central nervous system
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transcription factors. ZFPM2 protein's interaction with GATA4 is notable for controlling the
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were greatly elevated; these cases were associated with decreases cardiac tissue levels of
1148:-containing protein encoded by this gene is a widely expressed member of the FOG family of 494: 87: 1597:"Molecular cloning of FOG-2: a modulator of transcription factor GATA-4 in cardiomyocytes" 1420: 311: 2179: 1612: 1473:
in ZFPM2 protein and consequential failure of GATA4 to promote normal lung development.
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end of the ZFPM2 protein contains two domains, one of which interacts directly with the
2428: 2401: 2102: 2077: 2048: 2023: 1912: 1887: 1782: 1755: 50:, DIH3, FOG2, ZC2HC11B, ZNF89B, hFOG-2, SRXY9, zinc finger protein, FOG family member 2 2348: 2323: 2198: 2163: 2145: 2120: 743: 738: 733: 728: 723: 718: 713: 708: 703: 698: 693: 688: 683: 678: 673: 668: 663: 658: 653: 648: 643: 638: 633: 628: 623: 607: 602: 597: 581: 576: 571: 566: 561: 556: 551: 546: 541: 536: 2575: 2509: 1631: 1596: 1419:. Sporadic cases of Tetralogy of Fallot were also found in cases where the levels of 523: 2525: 2487: 2279: 1983:"CpG island shore methylation of ZFPM2 is identified in tetralogy of fallot samples" 1967: 71: 1481: 1454: 1301:
and, during the early stages of its development, the heart. Human ZFPM2 contains 8
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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
1343: 1302: 1294: 1179: 1145: 2470: 2453: 2402:"Fog2 is required for normal diaphragm and lung development in mice and humans" 2383: 2366: 2093: 1729: 412: 1951: 1772: 1327: 1298: 228: 125: 75: 1672: 1655: 1654:
Holmes M, Turner J, Fox A, Chisholm O, Crossley M, Chong B (September 1999).
2551: 2534: 1462: 773: 472: 350: 295: 282: 194: 181: 83: 2560: 2517: 2479: 2437: 2392: 2357: 2314: 2305: 2288: 2271: 2242: 2207: 2188: 2154: 2111: 2057: 2008: 1959: 1921: 1863: 1791: 1737: 1681: 1888:"Combinatorial regulation of tissue specification by GATA and FOG factors" 1825: 1808: 1640: 1621: 1319:
to inhibit its ability to stimulate the expression of a target gene in an
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gene are responsible for sporadic, very rare cases of a familial form of
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DNA-binding transcription repressor activity, RNA polymerase II-specific
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DNA-binding transcription factor activity, RNA polymerase II-specific
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expression in mice is also required for normal development of the
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Strausberg RL, Feingold EA, Grouse LH, et al. (2003).
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proteins. The NuRD complex and the CtBPs are classified as
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of various tissues, particularly the heart, diaphragm, and
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Sheng W, Chen L, Wang H, Ma X, Ma D, Huang G (July 2016).
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Crispino JD, Lodish MB, Thurberg BL, et al. (2001).
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positive regulation of transcription by RNA polymerase II
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negative regulation of transcription by RNA polymerase II
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Anttonen M, Ketola I, Parviainen H, et al. (2004).
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Svensson EC, Tufts RL, Polk CE, Leiden JM (March 1999).
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positive regulation of cardiac muscle cell proliferation
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Ackerman KG, Herron BJ, Vargas SO, et al. (2005).
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Gerhard DS, Wagner L, Feingold EA, et al. (2004).
1257:, is located on chromosome 15 and consists of 8 exons. 1699:"Entrez Gene: ZFPM2 zinc finger protein, multitype 2" 1457:
gene mutations are responsible for sporadic cases of
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gene is found in a wide range of animal species from
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right ventricular cardiac muscle tissue morphogenesis
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gene are responsible for rare and sporadic cases of
2533:Bleyl SB, Moshrefi A, Shaw GM, et al. (2007). 1803: 1801: 1308:and interacts directly with various members of the 1024: 995: 965: 936: 714:
negative regulation of transcription, DNA-templated
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positive regulation of transcription, DNA-templated
1538: 1536: 1534: 1517: 1515: 1513: 2365:Chan EM, Comer EM, Brown FC, et al. (2005). 266: 165: 2287:Hirai M, Ono K, Morimoto T, et al. (2004). 744:regulation of transcription by RNA polymerase II 1933: 1931: 1881: 1879: 1877: 1875: 1873: 1837: 1835: 1221:mutations are responsible for certain forms of 1193:The ZFPM2 protein interacts primarily with the 704:negative regulation of female gonad development 624:negative regulation of fat cell differentiation 16:Protein-coding gene in the species Homo sapiens 2076:Fox AH, Liew C, Holmes M, et al. (1999). 1749: 1747: 1710: 1708: 1543:GRCm38: Ensembl release 89: ENSMUSG00000022306 1465:and pulmonary vascular disorder that leads to 1820: 1818: 719:positive regulation of male gonad development 8: 2367:"AML1-FOG2 fusion protein in myelodysplasia" 1844:Seminars in Cell & Developmental Biology 1522:GRCh38: Ensembl release 89: ENSG00000169946 1190:sections of the various GATA target genes. 2452:Lim J, Hao T, Shaw C, et al. (2006). 1401:failure to from the pulmonary artery valve 769: 629:regulation of transcription, DNA-templated 519: 307: 206: 103: 2550: 2469: 2427: 2417: 2382: 2347: 2304: 2232: 2197: 2187: 2144: 2101: 2047: 1998: 1911: 1781: 1771: 1671: 1630: 1620: 1693: 1691: 1116:zinc finger protein, FOG family member 2 361:Skeletal muscle tissue of biceps brachii 1886:Chlon TM, Crispino JD (November 2012). 1509: 1120:Friend of GATA2, Friend of GATA-2, FOG2 1469:. These defects are considered due to 1174:genes in mice. Its members may act as 20: 381:cardiac muscle tissue of right atrium 271: 232: 227: 170: 129: 124: 7: 1718:European Journal of Medical Genetics 1413:transposition of the great arteries 1021: 992: 962: 933: 909: 890: 864: 845: 819: 800: 739:transcription by RNA polymerase II 684:outflow tract septum morphogenesis 547:transcription corepressor activity 542:transcription coactivator activity 489: 407: 345: 324: 14: 1130:that in humans is encoded by the 674:negative regulation of cell death 644:cardiac muscle tissue development 2510:10.1111/j.1399-0004.2007.00752.x 2443: 1459:congenital diaphragmatic hernias 1227:congenital diaphragmatic hernias 649:ventricular septum morphogenesis 493: 451:lumbar subsegment of spinal cord 255: 248: 242: 219: 154: 147: 141: 116: 2028:Disease Models & Mechanisms 1940:Molecular Genetics and Genomics 1496:. The disorder likely reflects 1447:Congenital diaphragmatic hernia 664:in utero embryonic development 504:More reference expression data 473:More reference expression data 1: 2234:10.1095/biolreprod.102.008599 1409:double outlet right ventricle 1253:. The equivalent mouse gene, 1156:. The family consists of the 240: 139: 2419:10.1371/journal.pgen.0010010 2168:Proc. Natl. Acad. Sci. U.S.A 1856:10.1016/j.semcdb.2004.10.006 1490:disorders of sex development 1182:to modulate the activity of 709:gonadal mesoderm development 679:transcription, DNA-templated 557:transcription factor binding 397:myocardium of left ventricle 2582:Genes on human chromosome 8 1233:in mice as well as humans. 634:embryonic organ development 2598: 2471:10.1016/j.cell.2006.03.032 2384:10.1182/blood-2004-07-2762 1730:10.1016/j.ejmg.2014.04.006 1184:GATA transcription factors 1952:10.1007/s00438-017-1373-6 1773:10.1186/s12887-016-0737-0 1578:"Mouse PubMed Reference:" 1560:"Human PubMed Reference:" 1405:ventricular septal defect 1391:. These include cases of 1310:GATA transcription factor 1112:Zinc finger protein ZFPM2 1098: 1093: 1089: 1082: 1066: 1047: 1028: 999: 988: 969: 940: 929: 916: 912: 897: 893: 884: 871: 867: 852: 848: 839: 826: 822: 807: 803: 794: 779: 772: 768: 752: 522: 518: 501: 492: 483: 470: 419: 410: 357: 348: 318: 310: 306: 289: 276: 239: 218: 209: 205: 188: 175: 138: 115: 106: 102: 57: 54: 44: 37: 32: 28: 23: 2094:10.1093/emboj/18.10.2812 1673:10.1074/jbc.274.33.23491 1601:Proc Natl Acad Sci U S A 1389:congenital heart disease 1379:Congenital heart disease 1267:heart ventricular muscle 1223:congenital heart defects 1060:Chr 15: 40.52 – 40.97 Mb 1053:Chr 8: 104.59 – 105.8 Mb 273:15 B3.1|15 15.74 cM 2552:10.1038/sj.ejhg.5201872 1417:interrupted aortic arch 373:vastus lateralis muscle 2306:10.1074/jbc.M401737200 2189:10.1073/pnas.242603899 1467:pulmonary hypertension 1285:, lung and diaphragm. 1271:atrioventricular canal 423:atrioventricular valve 385:triceps brachii muscle 1622:10.1073/pnas.96.3.956 1211:embryonic development 1154:transcription factors 234:Chromosome 15 (mouse) 1317:transcription factor 1166:genes in humans and 734:cell differentiation 577:nucleic acid binding 132:Chromosome 8 (human) 2180:2002PNAS...9916899M 1613:1999PNAS...96..956S 1494:ambiguous genitalia 1393:Tetralogy of Fallot 1275:tetralogy of Fallot 1231:ambiguous genitalia 1217:. Correspondingly, 1134:and in mice by the 431:endocardial cushion 365:germinal epithelium 2539:Eur. J. Hum. Genet 2340:10.1101/gr.2596504 2264:10.1002/humu.10261 2137:10.1101/gad.875201 2040:10.1242/dmm.028365 2000:10.1038/pr.2016.42 1987:Pediatric Research 1904:10.1242/dev.080440 1498:haploinsufficiency 1471:haploinsufficiency 1397:truncus arteriosus 1374:Clinical relevancy 1118:, but also termed 874:ENSMUSG00000022306 617:Biological process 591:Cellular component 530:Molecular function 435:lobe of cerebellum 2174:(26): 16899–903. 1484:mutations in the 1383:Mutations in the 1332:Mi-2/NuRD complex 1306:structural motifs 1109: 1108: 1105: 1104: 1078: 1077: 1043: 1042: 1018: 1017: 984: 983: 959: 958: 925: 924: 906: 905: 880: 879: 861: 860: 835: 834: 816: 815: 764: 763: 699:heart development 659:blood coagulation 562:metal ion binding 514: 513: 510: 509: 479: 478: 466: 465: 439:cerebellar vermis 404: 403: 302: 301: 201: 200: 96:ZFPM2 - orthologs 2589: 2564: 2554: 2529: 2491: 2473: 2448: 2447: 2441: 2431: 2421: 2396: 2386: 2361: 2351: 2318: 2308: 2299:(36): 37640–50. 2283: 2246: 2236: 2211: 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4523–6. 2362: 2319: 2284: 2247: 2227:(4): 1333–40. 2212: 2159: 2116: 2072: 2070: 2067: 2064: 2063: 2034:(8): 955–970. 2014: 1973: 1946:(1): 217–223. 1927: 1869: 1831: 1814: 1797: 1760:BMC Pediatrics 1743: 1704: 1687: 1646: 1587: 1569: 1551: 1530: 1508: 1507: 1505: 1502: 1478: 1475: 1448: 1445: 1403:combined with 1380: 1377: 1375: 1372: 1351: 1348: 1323:model system. 1290: 1287: 1277:malformation. 1238: 1235: 1197:but also with 1107: 1106: 1103: 1102: 1097: 1087: 1086: 1080: 1079: 1076: 1075: 1073: 1071: 1064: 1063: 1056: 1049: 1045: 1044: 1041: 1040: 1026: 1025: 1019: 1016: 1015: 997: 996: 990: 986: 985: 982: 981: 967: 966: 960: 957: 956: 938: 937: 931: 927: 926: 923: 922: 914: 913: 907: 904: 903: 895: 894: 888: 882: 881: 878: 877: 869: 868: 862: 859: 858: 850: 849: 843: 837: 836: 833: 832: 824: 823: 817: 814: 813: 805: 804: 798: 792: 791: 786: 781: 777: 776: 766: 765: 762: 761: 750: 749: 747: 746: 741: 736: 731: 726: 721: 716: 711: 706: 701: 696: 691: 689:vasculogenesis 686: 681: 676: 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2450: 2446: 2439: 2435: 2430: 2425: 2420: 2415: 2411: 2407: 2403: 2398: 2394: 2390: 2385: 2380: 2376: 2372: 2368: 2363: 2359: 2355: 2350: 2345: 2341: 2337: 2333: 2329: 2325: 2320: 2316: 2312: 2307: 2302: 2298: 2294: 2293:J. Biol. Chem 2290: 2285: 2281: 2277: 2273: 2269: 2265: 2261: 2257: 2253: 2248: 2244: 2240: 2235: 2230: 2226: 2222: 2218: 2213: 2209: 2205: 2200: 2195: 2190: 2185: 2181: 2177: 2173: 2169: 2165: 2160: 2156: 2152: 2147: 2142: 2138: 2134: 2131:(7): 839–44. 2130: 2126: 2122: 2117: 2113: 2109: 2104: 2099: 2095: 2091: 2087: 2083: 2079: 2074: 2073: 2068: 2059: 2055: 2050: 2045: 2041: 2037: 2033: 2029: 2025: 2018: 2015: 2010: 2006: 2001: 1996: 1992: 1988: 1984: 1977: 1974: 1969: 1965: 1961: 1957: 1953: 1949: 1945: 1941: 1934: 1932: 1928: 1923: 1919: 1914: 1909: 1905: 1901: 1897: 1893: 1889: 1882: 1880: 1878: 1876: 1874: 1870: 1865: 1861: 1857: 1853: 1850:(1): 117–28. 1849: 1845: 1838: 1836: 1832: 1827: 1821: 1819: 1815: 1810: 1804: 1802: 1798: 1793: 1789: 1784: 1779: 1774: 1769: 1765: 1761: 1757: 1750: 1748: 1744: 1739: 1735: 1731: 1727: 1724:(6): 247–52. 1723: 1719: 1711: 1709: 1705: 1700: 1694: 1692: 1688: 1683: 1679: 1674: 1669: 1665: 1661: 1657: 1650: 1647: 1642: 1638: 1633: 1628: 1623: 1618: 1614: 1610: 1607:(3): 956–61. 1606: 1602: 1598: 1591: 1588: 1583: 1579: 1573: 1570: 1565: 1561: 1555: 1552: 1548: 1544: 1539: 1537: 1535: 1531: 1527: 1523: 1518: 1516: 1514: 1510: 1503: 1501: 1499: 1495: 1491: 1487: 1483: 1476: 1474: 1472: 1468: 1464: 1460: 1456: 1453: 1446: 1444: 1442: 1438: 1434: 1430: 1426: 1422: 1418: 1414: 1410: 1406: 1402: 1398: 1394: 1390: 1386: 1378: 1373: 1371: 1369: 1365: 1361: 1357: 1349: 1347: 1345: 1341: 1337: 1333: 1329: 1324: 1322: 1318: 1315: 1311: 1307: 1304: 1300: 1296: 1288: 1286: 1284: 1280: 1276: 1272: 1268: 1264: 1260: 1256: 1252: 1248: 1244: 1236: 1234: 1232: 1228: 1224: 1220: 1216: 1212: 1208: 1204: 1200: 1196: 1191: 1189: 1185: 1181: 1177: 1173: 1169: 1165: 1161: 1160: 1155: 1151: 1147: 1142: 1140: 1137: 1133: 1129: 1125: 1121: 1117: 1113: 1101: 1096: 1092: 1088: 1085: 1081: 1074: 1072: 1069: 1065: 1061: 1057: 1054: 1050: 1046: 1039: 1037: 1033: 1027: 1023: 1020: 1014: 1012: 1008: 1004: 998: 994: 991: 987: 980: 978: 974: 968: 964: 961: 955: 953: 949: 945: 939: 935: 932: 930:RefSeq (mRNA) 928: 921: 920: 915: 911: 908: 902: 901: 896: 892: 889: 887: 883: 876: 875: 870: 866: 863: 857: 856: 851: 847: 844: 842: 838: 831: 830: 825: 821: 818: 812: 811: 806: 802: 799: 797: 793: 790: 787: 785: 782: 778: 775: 771: 767: 760: 756: 751: 745: 742: 740: 737: 735: 732: 730: 727: 725: 722: 720: 717: 715: 712: 710: 707: 705: 702: 700: 697: 695: 692: 690: 687: 685: 682: 680: 677: 675: 672: 670: 667: 665: 662: 660: 657: 655: 652: 650: 647: 645: 642: 640: 637: 635: 632: 630: 627: 625: 622: 621: 619: 616: 615: 609: 606: 604: 601: 599: 596: 595: 593: 590: 589: 583: 580: 578: 575: 573: 570: 568: 565: 563: 560: 558: 555: 553: 550: 548: 545: 543: 540: 538: 535: 534: 532: 529: 528: 525: 524:Gene ontology 521: 517: 505: 500: 496: 491: 488: 486: 482: 474: 469: 458: 454: 450: 447:Gonadal ridge 446: 442: 438: 434: 430: 426: 422: 421: 418: 414: 409: 406: 396: 392: 388: 384: 380: 376: 372: 368: 364: 360: 359: 356: 352: 347: 344: 343: 340: 338: 334: 332: 331: 327: 326: 323: 321: 317: 313: 309: 305: 297: 292: 288: 284: 279: 269: 265: 258: 251: 245: 238: 230: 226: 222: 217: 213: 208: 204: 196: 191: 187: 183: 178: 168: 164: 157: 150: 144: 137: 133: 127: 123: 119: 114: 110: 105: 101: 97: 93: 89: 85: 81: 77: 73: 69: 65: 61: 53: 48: 41: 36: 31: 27: 22: 19: 2568: 2545:(9): 950–8. 2542: 2538: 2501: 2497: 2461: 2457: 2412:(1): 58–65. 2409: 2405: 2374: 2370: 2331: 2327: 2296: 2292: 2258:(5): 372–7. 2255: 2251: 2224: 2221:Biol. Reprod 2220: 2171: 2167: 2128: 2124: 2085: 2081: 2031: 2027: 2017: 1993:(1): 151–8. 1990: 1986: 1976: 1943: 1939: 1895: 1891: 1847: 1843: 1763: 1759: 1721: 1717: 1663: 1659: 1649: 1604: 1600: 1590: 1581: 1572: 1563: 1554: 1485: 1482:Heterozygous 1480: 1455:heterozygous 1451: 1450: 1440: 1428: 1384: 1382: 1353: 1344:corepressors 1326:The extreme 1325: 1292: 1278: 1262: 1254: 1242: 1240: 1218: 1192: 1180:corepressors 1176:coactivators 1171: 1167: 1163: 1157: 1143: 1135: 1131: 1123: 1119: 1115: 1111: 1110: 1036:NP_001343927 1029: 1011:NP_001349766 1007:NP_001349765 1000: 977:NM_001356998 970: 952:NM_001362837 948:NM_001362836 941: 917: 898: 872: 853: 827: 808: 788: 783: 443:vas deferens 335: 328: 193:105,804,539 180:104,590,733 55:External IDs 18: 2498:Clin. Genet 1892:Development 1660:J Biol Chem 1303:zinc finger 1295:endometrium 1146:zinc finger 603:nucleoplasm 537:DNA binding 294:40,967,988 281:40,518,431 33:Identifiers 2406:PLOS Genet 2328:Genome Res 2252:Hum. Mutat 1766:(1): 195. 1549:, May 2017 1528:, May 2017 1504:References 1328:N terminal 1299:cerebellum 1273:, and the 1150:regulators 455:belly cord 339:(ortholog) 76:HomoloGene 2125:Genes Dev 1463:dysplasia 1425:CpG sites 1269:, common 1032:NP_035896 1003:NP_036214 973:NM_011766 944:NM_012082 774:Orthologs 598:cytoplasm 84:GeneCards 2576:Category 2561:17568391 2526:20572160 2518:17309641 2488:13709685 2480:16713569 2438:16103912 2393:15705784 2358:15489334 2315:15220332 2280:21531781 2272:14517948 2243:12606418 2208:12477932 2155:11297508 2112:10329627 2058:28768736 2009:26959486 1968:23888323 1960:29018978 1922:23048181 1864:15659346 1792:27899089 1738:24769157 1682:10438528 1545:– 1524:– 1433:promoter 1321:in vitro 1259:Knockout 1188:promoter 1084:Wikidata 753:Sources: 2429:1183529 2176:Bibcode 2103:1171362 2049:5560060 1913:3472596 1783:5129225 1641:9927675 1609:Bibcode 1547:Ensembl 1526:Ensembl 1427:in the 1289:Protein 1178:and/or 1128:protein 1126:, is a 1114:, i.e. 886:UniProt 841:Ensembl 780:Species 759:QuickGO 608:nucleus 314:pattern 72:1334444 40:Aliases 2559:  2524:  2516:  2486:  2478:  2436:  2426:  2391:  2356:  2349:528928 2346:  2313:  2278:  2270:  2241:  2206:  2199:139241 2196:  2153:  2146:312667 2143:  2110:  2100:  2082:EMBO J 2056:  2046:  2007:  1966:  1958:  1920:  1910:  1862:  1790:  1780:  1736:  1680:  1639:  1629:  1415:, and 1366:, and 1283:gonads 1229:, and 1215:gonads 1205:, and 1070:search 1068:PubMed 919:Q8CCH7 900:Q8WW38 796:Entrez 485:BioGPS 377:glutes 172:8q23.1 64:603693 2522:S2CID 2484:S2CID 2371:Blood 2276:S2CID 1964:S2CID 1632:15332 1486:ZFPM2 1452:ZFPM2 1441:ZFPM2 1431:gene 1429:ZFPM2 1385:ZFPM2 1368:GATA6 1364:GATA5 1360:GATA4 1356:GATA3 1340:CTBP2 1336:CTBP1 1314:GATA4 1279:ZFPM2 1263:ZFPM2 1255:Zfpm2 1251:exons 1247:flies 1243:ZFPM2 1219:ZFPM2 1207:GATA6 1203:GATA5 1199:GATA2 1195:GATA4 1172:Zfpm2 1168:Zfpm1 1164:ZFPM2 1159:ZFPM1 1136:Zfpm2 1132:ZFPM2 1124:FOG-2 1122:, or 829:22762 810:23414 789:Mouse 784:Human 755:Amigo 337:Mouse 330:Human 277:Start 212:Mouse 176:Start 109:Human 88:ZFPM2 47:ZFPM2 24:ZFPM2 2557:PMID 2514:PMID 2476:PMID 2458:Cell 2434:PMID 2389:PMID 2354:PMID 2311:PMID 2268:PMID 2239:PMID 2204:PMID 2151:PMID 2108:PMID 2054:PMID 2005:PMID 1956:PMID 1918:PMID 1860:PMID 1788:PMID 1734:PMID 1678:PMID 1637:PMID 1439:for 1437:mRNA 1241:The 1237:Gene 1170:and 1162:and 1144:The 1139:gene 389:pons 320:Bgee 268:Band 229:Chr. 167:Band 126:Chr. 80:8008 60:OMIM 2547:doi 2506:doi 2466:doi 2462:125 2424:PMC 2414:doi 2379:doi 2375:105 2344:PMC 2336:doi 2301:doi 2297:279 2260:doi 2229:doi 2194:PMC 2184:doi 2141:PMC 2133:doi 2098:PMC 2090:doi 2044:PMC 2036:doi 1995:doi 1948:doi 1944:293 1908:PMC 1900:doi 1896:139 1852:doi 1778:PMC 1768:doi 1726:doi 1668:doi 1664:274 1627:PMC 1617:doi 1423:at 1338:or 1261:of 1152:of 290:End 189:End 92:OMA 68:MGI 2578:: 2555:. 2543:15 2541:. 2537:. 2520:. 2512:. 2502:71 2500:. 2482:. 2474:. 2460:. 2456:. 2432:. 2422:. 2408:. 2404:. 2387:. 2373:. 2369:. 2352:. 2342:. 2332:14 2330:. 2326:. 2309:. 2295:. 2291:. 2274:. 2266:. 2256:22 2254:. 2237:. 2225:68 2223:. 2219:. 2202:. 2192:. 2182:. 2172:99 2170:. 2166:. 2149:. 2139:. 2129:15 2127:. 2123:. 2106:. 2096:. 2086:18 2084:. 2080:. 2052:. 2042:. 2032:10 2030:. 2026:. 2003:. 1991:80 1989:. 1985:. 1962:. 1954:. 1942:. 1930:^ 1916:. 1906:. 1894:. 1890:. 1872:^ 1858:. 1848:16 1846:. 1834:^ 1817:^ 1800:^ 1786:. 1776:. 1764:16 1762:. 1758:. 1746:^ 1732:. 1722:57 1720:. 1707:^ 1690:^ 1676:. 1662:. 1658:. 1635:. 1625:. 1615:. 1605:96 1603:. 1599:. 1580:. 1562:. 1533:^ 1512:^ 1492:, 1411:, 1407:, 1399:, 1395:, 1362:, 1358:, 1225:, 1201:, 1141:. 757:/ 296:bp 283:bp 195:bp 182:bp 90:; 86:: 82:; 78:: 74:; 70:: 66:; 62:: 2563:. 2549:: 2528:. 2508:: 2490:. 2468:: 2440:. 2416:: 2410:1 2395:. 2381:: 2360:. 2338:: 2317:. 2303:: 2282:. 2262:: 2245:. 2231:: 2210:. 2186:: 2178:: 2157:. 2135:: 2114:. 2092:: 2060:. 2038:: 2011:. 1997:: 1970:. 1950:: 1924:. 1902:: 1866:. 1854:: 1828:. 1811:. 1794:. 1770:: 1740:. 1728:: 1701:. 1684:. 1670:: 1643:. 1619:: 1611:: 1584:. 1566:. 214:) 111:) 94::

Index

Aliases
ZFPM2
OMIM
603693
MGI
1334444
HomoloGene
8008
GeneCards
ZFPM2
OMA
ZFPM2 - orthologs
Human
Chromosome 8 (human)
Chr.
Chromosome 8 (human)
Chromosome 8 (human)
Genomic location for ZFPM2
Genomic location for ZFPM2
Band
bp
bp
Mouse
Chromosome 15 (mouse)
Chr.
Chromosome 15 (mouse)
Genomic location for ZFPM2
Genomic location for ZFPM2
Band
bp

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