242:
219:
116:
141:
248:
147:
2245:
1608:
Bakkaloglu B, O'Roak BJ, Louvi A, Gupta AR, Abelson JF, Morgan TM, Chawarska K, Klin A, Ercan-Sencicek AG, Stillman AA, Tanriover G, Abrahams BS, Duvall JA, Robbins EM, Geschwind DH, Biederer T, Gunel M, Lifton RP, State MW (January 2008).
2026:
Denisenko-Nehrbass N, Oguievetskaia K, Goutebroze L, Galvez T, Yamakawa H, Ohara O, Carnaud M, Girault JA (January 2003). "Protein 4.1B associates with both Caspr/paranodin and Caspr2 at paranodes and juxtaparanodes of myelinated fibres".
1946:
Spiegel I, Salomon D, Erne B, Schaeren-Wiemers N, Peles E (June 2002). "Caspr3 and caspr4, two novel members of the caspr family are expressed in the nervous system and interact with PDZ domains".
1114:. It may play a role in the local differentiation of the axon into distinct functional subdomains. This gene encompasses almost 1.6% of chromosome 7 and is one of the largest genes in the
2064:
Verkerk AJ, Mathews CA, Joosse M, Eussen BH, Heutink P, Oostra BA (July 2003). "CNTNAP2 is disrupted in a family with Gilles de la
Tourette syndrome and obsessive compulsive disorder".
255:
154:
1326:"Prediction of the coding sequences of unidentified human genes. XII. The complete sequences of 100 new cDNA clones from brain which code for large proteins in vitro"
1469:
Alarcón M, Abrahams BS, Stone JL, Duvall JA, Perederiy JV, Bomar JM, Sebat J, Wigler M, Martin CL, Ledbetter DH, Nelson SF, Cantor RM, Geschwind DH (January 2008).
1517:
2136:
Fu GK, Wang JT, Yang J, Au-Young J, Stuve LL (July 2004). "Circular rapid amplification of cDNA ends for high-throughput extension cloning of partial genes".
1762:"CNTNAP2 and NRXN1 are mutated in autosomal-recessive Pitt-Hopkins-like mental retardation and determine the level of a common synaptic protein in Drosophila"
2093:
Traka M, Goutebroze L, Denisenko N, Bessa M, Nifli A, Havaki S, Iwakura Y, Fukamauchi F, Watanabe K, Soliven B, Girault JA, Karagogeos D (September 2003).
1809:
Traka M, Goutebroze L, Denisenko N, Bessa M, Nifli A, Havaki S, Iwakura Y, Fukamauchi F, Watanabe K, Soliven B, Girault JA, Karagogeos D (September 2003).
1662:
Vernes SC, Newbury DF, Abrahams BS, Winchester L, Nicod J, Groszer M, Alarcón M, Oliver PL, Davies KE, Geschwind DH, Monaco AP, Fisher SE (November 2008).
802:
783:
77:
1909:
Nakabayashi K, Scherer SW (April 2001). "The human contactin-associated protein-like 2 gene (CNTNAP2) spans over 2 Mb of DNA at chromosome 7q35".
1106:
repeats and laminin G domains. In addition, it includes an F5/8 type C domain, discoidin/neuropilin- and fibrinogen-like domains, thrombospondin
2314:
48:, AUTS15, CASPR2, CDFE, NRXN4, PTHSL1, contactin associated protein-like 2, contactin associated protein like 2, contactin associated protein 2
2290:
1257:
1239:
2309:
1985:"Protein-protein interactions between large proteins: two-hybrid screening using a functionally classified library composed of long cDNAs"
1277:"Caspr2, a new member of the neurexin superfamily, is localized at the juxtaparanodes of myelinated axons and associates with K+ channels"
1610:
1542:
1470:
1861:
1110:-like domains and a putative PDZ binding site. This protein is localized at the juxtaparanodes of myelinated axons and associated with
1014:
241:
1021:
218:
1368:
1226:
1205:
2095:"Association of TAG-1 with Caspr2 is essential for the molecular organization of juxtaparanodal regions of myelinated fibers"
1867:
1811:"Association of TAG-1 with Caspr2 is essential for the molecular organization of juxtaparanodal regions of myelinated fibers"
1427:"Collisions between replication and transcription complexes cause common fragile site instability at the longest human genes"
1222:
1541:
Arking DE, Cutler DJ, Brune CW, Teslovich TM, West K, Ikeda M, Rea A, Guy M, Lin S, Cook EH, Chakravarti A (January 2008).
140:
115:
1201:
1324:
Nagase T, Ishikawa K, Suyama M, Kikuno R, Hirosawa M, Miyajima N, Tanaka A, Kotani H, Nomura N, Ohara O (December 1998).
1138:
57:
1525:
254:
153:
1161:
2202:"Disruption of the CNTNAP2 gene in a t(7;15) translocation family without symptoms of Gilles de la Tourette syndrome"
1611:"Molecular cytogenetic analysis and resequencing of contactin associated protein-like 2 in autism spectrum disorders"
247:
146:
1149:
2283:
2200:
Belloso JM, Bache I, Guitart M, Caballin MR, Halgren C, Kirchhoff M, Ropers HH, Tommerup N, Tümer Z (June 2007).
2165:
Strauss KA, Puffenberger EG, Huentelman MJ, Gottlieb S, Dobrin SE, Parod JM, Stephan DA, Morton DH (March 2006).
1426:
1275:
Poliak S, Gollan L, Martinez R, Custer A, Einheber S, Salzer JL, Trimmer JS, Shrager P, Peles E (December 1999).
1130:
851:
65:
1103:
832:
828:
1099:
1543:"A common genetic variant in the neurexin superfamily member CNTNAP2 increases familial risk of autism"
1471:"Linkage, association, and gene-expression analyses identify CNTNAP2 as an autism-susceptibility gene"
2276:
129:
44:
1873:
1588:
993:
942:
2052:
1971:
1934:
1407:
1306:
89:
997:
972:
946:
921:
1760:
Zweier C, de Jong EK, Zweier M, Orrico A, Ousager LB, Collins AL, et al. (November 2009).
2223:
2188:
2153:
2124:
2081:
2044:
2014:
1963:
1926:
1880:
1840:
1791:
1742:
1693:
1640:
1572:
1500:
1451:
1399:
1347:
1298:
1111:
37:
2260:
1118:. It may represent a positional candidate gene for the DFNB13 form of nonsyndromic deafness.
85:
2213:
2178:
2145:
2114:
2106:
2073:
2036:
2004:
1996:
1955:
1918:
1830:
1822:
1781:
1773:
1732:
1724:
1683:
1675:
1630:
1622:
1562:
1554:
1490:
1482:
1441:
1391:
1337:
1288:
334:
265:
209:
164:
1648:
1580:
1508:
309:
2119:
2094:
1835:
1810:
1786:
1761:
1737:
1712:
1688:
1663:
1635:
1567:
1495:
1177:
2077:
2009:
1984:
1293:
1276:
717:
712:
707:
702:
697:
692:
687:
682:
677:
672:
667:
662:
657:
652:
647:
642:
637:
632:
616:
611:
606:
601:
596:
591:
586:
581:
576:
571:
566:
561:
556:
551:
546:
530:
525:
2303:
2167:"Recessive symptomatic focal epilepsy and mutant contactin-associated protein-like 2"
2040:
1889:
512:
2056:
1975:
1938:
1310:
69:
2256:
1411:
1115:
327:
106:
1446:
93:
2149:
1262:
National Center for
Biotechnology Information, U.S. National Library of Medicine
1244:
National Center for
Biotechnology Information, U.S. National Library of Medicine
1777:
1626:
1558:
1486:
410:
1107:
226:
123:
73:
1664:"A functional genetic link between distinct developmental language disorders"
1342:
1325:
2218:
2201:
1202:
ENSG00000278728 GRCh38: Ensembl release 89: ENSG00000174469, ENSG00000278728
747:
470:
348:
293:
280:
192:
179:
81:
2227:
2192:
2157:
2128:
2085:
2048:
2018:
1967:
1959:
1930:
1922:
1844:
1795:
1746:
1697:
1644:
1576:
1504:
1455:
1403:
1351:
1302:
2110:
1826:
1679:
1061:
1056:
2183:
2166:
1095:
1045:
896:
877:
1395:
1894:
1884:
1077:
863:
814:
2000:
1728:
1088:
1029:
769:
2244:
1102:
and receptors. This protein, like other neurexin proteins, contains
1165:
732:
728:
2252:
1382:
Ashley, Euan A. (16 August 2016). "Towards precision medicine".
1084:
61:
1879:
Overview of all the structural information available in the
1098:
family which functions in the vertebrate nervous system as
1369:"Entrez Gene: CNTNAP2 contactin associated protein-like 2"
1091:
GRCh38, CNTNAP2 is the longest gene in the human genome
317:
2264:
1518:"UCLA scientists identify new genetic link to autism"
482:
1589:"Hopkins Team Identifies Autism Susceptibility Gene"
713:
protein localization to juxtaparanode region of axon
986:
965:
935:
914:
1218:
1216:
1214:
1197:
1195:
1193:
1425:Helmrich A, Ballarino M, Tora L (December 2011).
264:
163:
1983:Nakayama M, Kikuno R, Ohara O (November 2002).
1223:GRCm38: Ensembl release 89: ENSMUSG00000039419
633:clustering of voltage-gated potassium channels
2284:
1893:(Contactin-associated protein-like 2) at the
8:
2291:
2277:
743:
508:
449:transitional epithelium of urinary bladder
305:
204:
101:
2217:
2182:
2118:
2008:
1834:
1785:
1736:
1687:
1634:
1566:
1494:
1445:
1341:
1292:
1137:may also be related to a disorder called
1363:
1361:
1087:. Since the most recent reference human
1189:
607:voltage-gated potassium channel complex
18:
269:
230:
225:
168:
127:
122:
7:
2241:
2239:
2029:The European Journal of Neuroscience
1948:Molecular and Cellular Neurosciences
1148:result in a disorder that resembles
425:vestibular membrane of cochlear duct
2171:The New England Journal of Medicine
1711:Peippo M, Ignatius J (April 2012).
1668:The New England Journal of Medicine
1074:Contactin-associated protein-like 2
698:superior temporal gyrus development
2263:. You can help Knowledge (XXG) by
2206:European Journal of Human Genetics
1766:American Journal of Human Genetics
1615:American Journal of Human Genetics
1547:American Journal of Human Genetics
1475:American Journal of Human Genetics
1094:This gene encodes a member of the
983:
962:
932:
911:
887:
868:
842:
819:
793:
774:
487:
405:
343:
322:
14:
1133:but accounts for very few cases.
1080:that in humans is encoded by the
2243:
2041:10.1046/j.1460-9568.2003.02441.x
253:
246:
240:
217:
152:
145:
139:
114:
1180:, geneticist and neuroscientist
718:neuron projection morphogenesis
592:integral component of membrane
471:More reference expression data
1:
2315:Human chromosome 7 gene stubs
2078:10.1016/S0888-7543(03)00097-1
1516:Elaine Schmidt (2008-01-10).
1294:10.1016/S0896-6273(00)81049-1
703:neuron projection development
643:transmission of nerve impulse
238:
137:
16:Protein-coding gene in humans
1595:(Press release). 2008-01-22.
1447:10.1016/j.molcel.2011.10.013
1139:specific language impairment
587:juxtaparanode region of axon
2310:Genes on human chromosome 7
2150:10.1016/j.ygeno.2004.01.011
2099:The Journal of Cell Biology
1815:The Journal of Cell Biology
688:cerebral cortex development
2331:
2238:
1872:gene details page in the
1778:10.1016/j.ajhg.2009.10.004
1627:10.1016/j.ajhg.2007.09.017
1559:10.1016/j.ajhg.2007.09.015
1487:10.1016/j.ajhg.2007.09.005
1160:CNTNAP2 has been shown to
429:retinal pigment epithelium
1258:"Mouse PubMed Reference:"
1240:"Human PubMed Reference:"
1129:has been associated with
1060:
1055:
1051:
1044:
1028:
1015:Chr 7: 146.12 – 148.42 Mb
1009:
990:
969:
958:
939:
918:
907:
894:
890:
875:
871:
862:
849:
845:
826:
822:
813:
800:
796:
781:
777:
768:
753:
746:
742:
726:
648:limbic system development
511:
507:
495:
490:
481:
468:
417:
408:
391:anterior cingulate cortex
355:
346:
316:
308:
304:
287:
274:
237:
216:
207:
203:
186:
173:
136:
113:
104:
100:
55:
52:
42:
35:
30:
26:
21:
1131:autism spectrum disorder
2219:10.1038/sj.ejhg.5201824
1713:"Pitt-Hopkins Syndrome"
1384:Nature Reviews Genetics
1144:Recessive mutations in
1104:epidermal growth factor
1100:cell adhesion molecules
1022:Chr 6: 45.04 – 47.28 Mb
1960:10.1006/mcne.2002.1110
1923:10.1006/geno.2001.6517
1717:Molecular Syndromology
1593:Johns Hopkins Medicine
1343:10.1093/dnares/5.6.355
363:superior frontal gyrus
2111:10.1083/jcb.200305078
1827:10.1083/jcb.200305078
1680:10.1056/NEJMoa0802828
1150:Pitt–Hopkins syndrome
1122:Clinical significance
673:vocalization behavior
371:primary visual cortex
2184:10.1056/NEJMoa052773
1866:genome location and
708:striatum development
638:thalamus development
437:lateral hypothalamus
232:Chromosome 6 (mouse)
130:Chromosome 7 (human)
1874:UCSC Genome Browser
1396:10.1038/nrg.2016.86
383:ganglionic eminence
271:6|6 B2.2- B2.3
94:CNTNAP2 - orthologs
2251:This article on a
1112:potassium channels
852:ENSMUSG00000039419
658:neuron recognition
626:Biological process
617:paranodal junction
567:neuronal cell body
540:Cellular component
519:Molecular function
445:olfactory tubercle
387:right frontal lobe
2272:
2271:
2001:10.1101/gr.406902
1729:10.1159/000335287
1071:
1070:
1067:
1066:
1040:
1039:
1005:
1004:
980:
979:
954:
953:
929:
928:
903:
902:
884:
883:
858:
857:
839:
838:
809:
808:
790:
789:
738:
737:
668:brain development
503:
502:
499:
498:
477:
476:
464:
463:
457:nucleus accumbens
402:
401:
375:prefrontal cortex
300:
299:
199:
198:
2322:
2293:
2286:
2279:
2247:
2240:
2231:
2221:
2196:
2186:
2161:
2132:
2122:
2089:
2060:
2022:
2012:
1979:
1942:
1849:
1848:
1838:
1806:
1800:
1799:
1789:
1757:
1751:
1750:
1740:
1723:(3–5): 171–180.
1708:
1702:
1701:
1691:
1659:
1653:
1652:
1647:. Archived from
1638:
1605:
1599:
1596:
1584:
1579:. Archived from
1570:
1538:
1532:
1529:
1524:. Archived from
1512:
1507:. Archived from
1498:
1466:
1460:
1459:
1449:
1431:
1422:
1416:
1415:
1379:
1373:
1372:
1365:
1356:
1355:
1345:
1321:
1315:
1314:
1296:
1272:
1266:
1265:
1254:
1248:
1247:
1236:
1230:
1220:
1209:
1199:
1053:
1052:
1024:
1017:
1000:
984:
975:
963:
959:RefSeq (protein)
949:
933:
924:
912:
888:
869:
843:
820:
794:
775:
744:
509:
488:
473:
421:substantia nigra
413:
411:Top expressed in
406:
395:substantia nigra
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:
47:
40:
19:
2330:
2329:
2325:
2324:
2323:
2321:
2320:
2319:
2300:
2299:
2298:
2297:
2236:
2234:
2199:
2164:
2135:
2092:
2063:
2025:
1995:(11): 1773–84.
1989:Genome Research
1982:
1945:
1908:
1904:
1902:Further reading
1857:
1852:
1808:
1807:
1803:
1759:
1758:
1754:
1710:
1709:
1705:
1674:(22): 2337–45.
1661:
1660:
1656:
1607:
1606:
1602:
1587:
1540:
1539:
1535:
1515:
1468:
1467:
1463:
1429:
1424:
1423:
1419:
1381:
1380:
1376:
1367:
1366:
1359:
1323:
1322:
1318:
1274:
1273:
1269:
1256:
1255:
1251:
1238:
1237:
1233:
1221:
1212:
1200:
1191:
1187:
1174:
1158:
1124:
1062:View/Edit Mouse
1057:View/Edit Human
1020:
1013:
1010:Location (UCSC)
996:
992:
971:
945:
941:
920:
833:ENSG00000278728
831:
829:ENSG00000174469
722:
693:social behavior
621:
557:cell projection
552:Golgi apparatus
535:
531:protein binding
469:
460:
455:
451:
447:
443:
439:
435:
431:
427:
423:
409:
398:
393:
389:
385:
381:
379:Brodmann area 9
377:
373:
369:
365:
361:
359:corpus callosum
347:
291:
278:
270:
260:
259:
258:
251:
231:
208:Gene location (
190:
177:
169:
159:
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157:
150:
128:
105:Gene location (
56:
43:
36:
17:
12:
11:
5:
2328:
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2318:
2317:
2312:
2302:
2301:
2296:
2295:
2288:
2281:
2273:
2270:
2269:
2248:
2233:
2232:
2197:
2177:(13): 1370–7.
2162:
2133:
2105:(6): 1161–72.
2090:
2061:
2023:
1980:
1943:
1905:
1903:
1900:
1899:
1898:
1877:
1856:
1855:External links
1853:
1851:
1850:
1821:(6): 1161–72.
1801:
1752:
1703:
1654:
1651:on 2008-01-16.
1600:
1598:
1597:
1583:on 2008-01-16.
1533:
1531:
1530:
1528:on 2008-01-17.
1511:on 2008-01-16.
1461:
1434:Molecular Cell
1417:
1390:(9): 507–522.
1374:
1357:
1316:
1287:(4): 1037–47.
1267:
1249:
1231:
1210:
1188:
1186:
1183:
1182:
1181:
1178:Brett Abrahams
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683:adult behavior
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663:vocal learning
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577:early endosome
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526:enzyme binding
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310:RNA expression
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6:
4:
3:
2:
2327:
2316:
2313:
2311:
2308:
2307:
2305:
2294:
2289:
2287:
2282:
2280:
2275:
2274:
2268:
2266:
2262:
2258:
2254:
2249:
2246:
2242:
2237:
2229:
2225:
2220:
2215:
2211:
2207:
2203:
2198:
2194:
2190:
2185:
2180:
2176:
2172:
2168:
2163:
2159:
2155:
2151:
2147:
2144:(1): 205–10.
2143:
2139:
2134:
2130:
2126:
2121:
2116:
2112:
2108:
2104:
2100:
2096:
2091:
2087:
2083:
2079:
2075:
2071:
2067:
2062:
2058:
2054:
2050:
2046:
2042:
2038:
2034:
2030:
2024:
2020:
2016:
2011:
2006:
2002:
1998:
1994:
1990:
1986:
1981:
1977:
1973:
1969:
1965:
1961:
1957:
1954:(2): 283–97.
1953:
1949:
1944:
1940:
1936:
1932:
1928:
1924:
1920:
1917:(1): 108–12.
1916:
1912:
1907:
1906:
1901:
1896:
1892:
1891:
1886:
1882:
1878:
1875:
1871:
1870:
1865:
1864:
1859:
1858:
1854:
1846:
1842:
1837:
1832:
1828:
1824:
1820:
1816:
1812:
1805:
1802:
1797:
1793:
1788:
1783:
1779:
1775:
1772:(5): 655–66.
1771:
1767:
1763:
1756:
1753:
1748:
1744:
1739:
1734:
1730:
1726:
1722:
1718:
1714:
1707:
1704:
1699:
1695:
1690:
1685:
1681:
1677:
1673:
1669:
1665:
1658:
1655:
1650:
1646:
1642:
1637:
1632:
1628:
1624:
1621:(1): 165–73.
1620:
1616:
1612:
1604:
1601:
1594:
1590:
1586:
1585:
1582:
1578:
1574:
1569:
1564:
1560:
1556:
1552:
1548:
1544:
1537:
1534:
1527:
1523:
1522:UCLA Newsroom
1519:
1514:
1513:
1510:
1506:
1502:
1497:
1492:
1488:
1484:
1480:
1476:
1472:
1465:
1462:
1457:
1453:
1448:
1443:
1440:(6): 966–77.
1439:
1435:
1428:
1421:
1418:
1413:
1409:
1405:
1401:
1397:
1393:
1389:
1385:
1378:
1375:
1370:
1364:
1362:
1358:
1353:
1349:
1344:
1339:
1336:(6): 355–64.
1335:
1331:
1327:
1320:
1317:
1312:
1308:
1304:
1300:
1295:
1290:
1286:
1282:
1278:
1271:
1268:
1263:
1259:
1253:
1250:
1245:
1241:
1235:
1232:
1228:
1224:
1219:
1217:
1215:
1211:
1207:
1203:
1198:
1196:
1194:
1190:
1184:
1179:
1176:
1175:
1171:
1169:
1167:
1163:
1155:
1153:
1151:
1147:
1142:
1140:
1136:
1132:
1128:
1121:
1119:
1117:
1113:
1109:
1105:
1101:
1097:
1092:
1090:
1086:
1083:
1079:
1075:
1063:
1058:
1054:
1050:
1047:
1043:
1036:
1034:
1031:
1027:
1023:
1019:
1016:
1012:
1008:
1001:
999:
995:
989:
985:
982:
976:
974:
968:
964:
961:
957:
950:
948:
944:
938:
934:
931:
925:
923:
917:
913:
910:
908:RefSeq (mRNA)
906:
899:
898:
893:
889:
886:
880:
879:
874:
870:
867:
865:
861:
854:
853:
848:
844:
841:
835:
834:
830:
825:
821:
818:
816:
812:
805:
804:
799:
795:
792:
786:
785:
780:
776:
773:
771:
767:
764:
761:
759:
756:
752:
749:
745:
741:
734:
730:
725:
719:
716:
714:
711:
709:
706:
704:
701:
699:
696:
694:
691:
689:
686:
684:
681:
679:
678:cell adhesion
676:
674:
671:
669:
666:
664:
661:
659:
656:
654:
651:
649:
646:
644:
641:
639:
636:
634:
631:
630:
628:
625:
624:
618:
615:
613:
612:cell junction
610:
608:
605:
603:
600:
598:
595:
593:
590:
588:
585:
583:
580:
578:
575:
573:
570:
568:
565:
563:
560:
558:
555:
553:
550:
548:
545:
544:
542:
539:
538:
532:
529:
527:
524:
523:
521:
518:
517:
514:
513:Gene ontology
510:
506:
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:
2265:expanding it
2257:chromosome 7
2250:
2235:
2212:(6): 711–3.
2209:
2205:
2174:
2170:
2141:
2137:
2102:
2098:
2069:
2065:
2035:(2): 411–6.
2032:
2028:
1992:
1988:
1951:
1947:
1914:
1910:
1888:
1868:
1862:
1818:
1814:
1804:
1769:
1765:
1755:
1720:
1716:
1706:
1671:
1667:
1657:
1649:the original
1618:
1614:
1603:
1592:
1581:the original
1553:(1): 160–4.
1550:
1546:
1536:
1526:the original
1521:
1509:the original
1481:(1): 150–9.
1478:
1474:
1464:
1437:
1433:
1420:
1387:
1383:
1377:
1333:
1330:DNA Research
1329:
1319:
1284:
1280:
1270:
1261:
1252:
1243:
1234:
1159:
1156:Interactions
1145:
1143:
1134:
1126:
1125:
1116:human genome
1093:
1081:
1073:
1072:
994:NP_001004357
991:
970:
943:NM_001004357
940:
919:
895:
876:
850:
827:
801:
782:
762:
757:
562:cell surface
453:motor neuron
333:
326:
191:148,420,998
178:146,116,002
53:External IDs
292:47,281,147
279:45,036,291
31:Identifiers
2304:Categories
2072:(1): 1–9.
1229:, May 2017
1208:, May 2017
1185:References
1108:N-terminal
547:perikaryon
367:C1 segment
337:(ortholog)
170:7q35-q36.1
74:HomoloGene
2255:on human
998:NP_080047
973:NP_054860
947:NM_025771
922:NM_014141
748:Orthologs
82:GeneCards
2228:17392702
2193:16571880
2158:15203218
2138:Genomics
2129:12975355
2086:12809671
2066:Genomics
2057:21570541
2049:12542678
2019:12421765
1976:25024421
1968:12093160
1939:16120451
1931:11352571
1911:Genomics
1845:12975355
1796:19896112
1747:22670138
1698:18987363
1645:18179895
1577:18179894
1505:18179893
1456:22195969
1404:27528417
1352:10048485
1311:12444497
1303:10624965
1225:–
1204:–
1172:See also
1162:interact
1096:neurexin
1046:Wikidata
727:Sources:
653:learning
597:membrane
582:axolemma
572:dendrite
441:habenula
2120:2172849
1895:PDBe-KB
1885:UniProt
1869:CNTNAP2
1863:CNTNAP2
1836:2172849
1787:2775834
1738:3366706
1689:2756409
1636:2253974
1568:2253968
1496:2253955
1412:2609065
1227:Ensembl
1206:Ensembl
1146:CNTNAP2
1135:CNTNAP2
1127:CNTNAP2
1082:CNTNAP2
1078:protein
864:UniProt
815:Ensembl
754:Species
733:QuickGO
312:pattern
86:CNTNAP2
70:1914047
45:CNTNAP2
38:Aliases
22:CNTNAP2
2226:
2191:
2156:
2127:
2117:
2084:
2055:
2047:
2017:
2010:187542
2007:
1974:
1966:
1937:
1929:
1890:Q9UHC6
1860:Human
1843:
1833:
1794:
1784:
1745:
1735:
1696:
1686:
1643:
1633:
1575:
1565:
1503:
1493:
1454:
1410:
1402:
1350:
1309:
1301:
1281:Neuron
1089:genome
1032:search
1030:PubMed
897:Q9CPW0
878:Q9UHC6
770:Entrez
483:BioGPS
62:604569
2259:is a
2053:S2CID
1972:S2CID
1935:S2CID
1430:(PDF)
1408:S2CID
1307:S2CID
1166:CNTN2
1164:with
1076:is a
803:66797
784:26047
763:Mouse
758:Human
729:Amigo
433:molar
335:Mouse
328:Human
275:Start
210:Mouse
174:Start
107:Human
78:69159
2261:stub
2253:gene
2224:PMID
2189:PMID
2154:PMID
2125:PMID
2082:PMID
2045:PMID
2015:PMID
1964:PMID
1927:PMID
1883:for
1841:PMID
1792:PMID
1743:PMID
1694:PMID
1641:PMID
1573:PMID
1501:PMID
1452:PMID
1400:PMID
1348:PMID
1299:PMID
1085:gene
602:axon
318:Bgee
266:Band
227:Chr.
165:Band
124:Chr.
58:OMIM
2214:doi
2179:doi
2175:354
2146:doi
2115:PMC
2107:doi
2103:162
2074:doi
2037:doi
2005:PMC
1997:doi
1956:doi
1919:doi
1881:PDB
1831:PMC
1823:doi
1819:162
1782:PMC
1774:doi
1733:PMC
1725:doi
1684:PMC
1676:doi
1672:359
1631:PMC
1623:doi
1563:PMC
1555:doi
1491:PMC
1483:doi
1442:doi
1392:doi
1338:doi
1289:doi
491:n/a
288:End
187:End
90:OMA
66:MGI
2306::
2222:.
2210:15
2208:.
2204:.
2187:.
2173:.
2169:.
2152:.
2142:84
2140:.
2123:.
2113:.
2101:.
2097:.
2080:.
2070:82
2068:.
2051:.
2043:.
2033:17
2031:.
2013:.
2003:.
1993:12
1991:.
1987:.
1970:.
1962:.
1952:20
1950:.
1933:.
1925:.
1915:73
1913:.
1887::
1839:.
1829:.
1817:.
1813:.
1790:.
1780:.
1770:85
1768:.
1764:.
1741:.
1731:.
1719:.
1715:.
1692:.
1682:.
1670:.
1666:.
1639:.
1629:.
1619:82
1617:.
1613:.
1591:.
1571:.
1561:.
1551:82
1549:.
1545:.
1520:.
1499:.
1489:.
1479:82
1477:.
1473:.
1450:.
1438:44
1436:.
1432:.
1406:.
1398:.
1388:17
1386:.
1360:^
1346:.
1332:.
1328:.
1305:.
1297:.
1285:24
1283:.
1279:.
1260:.
1242:.
1213:^
1192:^
1168:.
1152:.
1141:.
731:/
294:bp
281:bp
193:bp
180:bp
88:;
84::
80:;
76::
72:;
68::
64:;
60::
2292:e
2285:t
2278:v
2267:.
2230:.
2216::
2195:.
2181::
2160:.
2148::
2131:.
2109::
2088:.
2076::
2059:.
2039::
2021:.
1999::
1978:.
1958::
1941:.
1921::
1897:.
1876:.
1847:.
1825::
1798:.
1776::
1749:.
1727::
1721:2
1700:.
1678::
1625::
1557::
1485::
1458:.
1444::
1414:.
1394::
1371:.
1354:.
1340::
1334:5
1313:.
1291::
1264:.
1246:.
212:)
109:)
92::
Text is available under the Creative Commons Attribution-ShareAlike License. Additional terms may apply.
