205:
182:
456:
1740:
211:
31:
1945:
1218:
Schollen E, Pardon E, Heykants L, Renard J, Doggett NA, Callen DF, Cassiman JJ, Matthijs G (February 1998). "Comparative analysis of the phosphomannomutase genes PMM1, PMM2 and PMM2psi: the sequence variation in the processed pseudogene is a reflection of the mutations found in the functional gene".
1161:
Martinsson T, Bjursell C, Stibler H, Kristiansson B, Skovby F, Jaeken J, Blennow G, Strömme P, Hanefeld F, Wahlström J (November 1994). "Linkage of a locus for carbohydrate-deficient glycoprotein syndrome type I (CDG1) to chromosome 16p, and linkage disequilibrium to microsatellite marker D16S406".
57:
1399:
Vuillaumier-Barrot S, Barnier A, Cuer M, Durand G, Grandchamp B, Seta N (December 1999). "Characterization of the 415G>A (E139K) PMM2 mutation in carbohydrate-deficient glycoprotein syndrome type Ia disrupting a splicing enhancer resulting in exon 5 skipping".
1037:
Matthijs G, Schollen E, Pardon E, Veiga-Da-Cunha M, Jaeken J, Cassiman JJ, Van
Schaftingen E (May 1997). "Mutations in PMM2, a phosphomannomutase gene on chromosome 16p13, in carbohydrate-deficient glycoprotein type I syndrome (Jaeken syndrome)".
1361:
Kondo I, Mizugishi K, Yoneda Y, Hashimoto T, Kuwajima K, Yuasa I, Shigemoto K, Kuroda Y (January 1999). "Missense mutations in phosphomannomutase 2 gene in two
Japanese families with carbohydrate-deficient glycoprotein syndrome type 1".
1472:
Imtiaz F, Worthington V, Champion M, Beesley C, Charlwood J, Clayton P, Keir G, Mian N, Winchester B (March 2000). "Genotypes and phenotypes of patients in the UK with carbohydrate-deficient glycoprotein syndrome type 1".
218:
1553:
Matthijs G, Schollen E, Bjursell C, Erlandson A, Freeze H, Imtiaz F, Kjaergaard S, Martinsson T, Schwartz M, Seta N, Vuillaumier-Barrot S, Westphal V, Winchester B (November 2000).
1639:
Westphal V, Enns GM, McCracken MF, Freeze HH (May 2001). "Functional analysis of novel mutations in a congenital disorder of glycosylation Ia patient with mixed Asian ancestry".
956:
necessary for the synthesis of dolichol-P-oligosaccharides. Mutations in the gene have been shown to cause defects in the protein glycosylation pathway which manifest as the
1771:
GeneReviews/NIH/NCBI/UW entry on PMM2-CDG (CDG-Ia)Carbohydrate-Deficient
Glycoprotein Syndrome, Type 1a; Congenital Disorder of Glycosylation Type 1a; Jaeken Syndrome
1103:
Matthijs G, Schollen E, Heykants L, GrĂĽnewald S (October 1999). "Phosphomannomutase deficiency: the molecular basis of the classical Jaeken syndrome (CDGS type Ia)".
1852:
659:
640:
143:
1668:
Heykants L, Schollen E, GrĂĽnewald S, Matthijs G (May 2001). "Identification and localization of two mouse phosphomannomutase genes, Pmm1 and Pmm2".
1328:"Detailed mapping of the phosphomannomutase 2 (PMM2) gene and mutation detection enable improved analysis for Scandinavian CDG type I families"
1019:
1001:
1903:
1828:
1510:
Vuillaumier-Barrot S, Hetet G, Barnier A, Dupré T, Cuer M, de Lonlay P, Cormier-Daire V, Durand G, Grandchamp B, Seta N (August 2000).
1413:
1293:"Absence of homozygosity for predominant mutations in PMM2 in Danish patients with carbohydrate-deficient glycoprotein syndrome type 1"
1776:
OMIM entries on
Carbohydrate-Deficient Glycoprotein Syndrome, Type 1a; Congenital Disorder of Glycosylation Type 1a; Jaeken Syndrome
1598:"PMM2 mutation spectrum, including 10 novel mutations, in a large CDG type 1A family material with a focus on Scandinavian families"
870:
1739:
2014:
1084:
1990:
1439:"Carbohydrate-deficient glycoprotein syndrome type 1A: expression and characterisation of wild type and mutant PMM2 in E. coli"
1719:
1614:
1597:
1571:
1554:
984:
957:
54:
1596:
Bjursell C, Erlandson A, Nordling M, Nilsson S, Wahlström J, Stibler H, Kristiansson B, Martinsson T (November 2000).
204:
1802:
181:
1250:"Lack of homozygotes for the most frequent disease allele in carbohydrate-deficient glycoprotein syndrome type 1A"
988:
1512:"Identification of four novel PMM2 mutations in congenital disorders of glycosylation (CDG) Ia French patients"
702:
123:
1185:"PMM (PMM1), the human homologue of SEC53 or yeast phosphomannomutase, is localized on chromosome 22q13"
1983:
1893:
1866:
217:
1842:
1712:
210:
110:
1927:
1819:
848:
797:
131:
1861:
1837:
844:
823:
793:
772:
1976:
1912:
1795:
1326:
Bjursell C, Wahlström J, Berg K, Stibler H, Kristiansson B, Matthijs G, Martinsson T (1999).
1183:
Matthijs G, Schollen E, Pirard M, Budarf ML, Van
Schaftingen E, Cassiman JJ (February 1997).
2009:
1705:
151:
8:
1917:
949:
945:
1876:
1871:
1627:
1584:
1536:
1511:
1498:
1425:
1387:
1274:
1249:
1063:
155:
1681:
1555:"Mutations in PMM2 that cause congenital disorders of glycosylation, type Ia (CDG-Ia)"
1375:
574:
569:
564:
559:
554:
538:
533:
528:
523:
507:
502:
497:
1685:
1656:
1619:
1576:
1541:
1490:
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1417:
1379:
1349:
1314:
1279:
1236:
1206:
1171:
1149:
1120:
1055:
103:
47:
1631:
1588:
1502:
1429:
1391:
1067:
135:
1788:
1677:
1648:
1609:
1566:
1531:
1523:
1482:
1450:
1409:
1371:
1339:
1304:
1269:
1261:
1228:
1196:
1141:
1112:
1047:
297:
228:
172:
1775:
1145:
1922:
960:
272:
1024:
National Center for
Biotechnology Information, U.S. National Library of Medicine
1006:
National Center for
Biotechnology Information, U.S. National Library of Medicine
1960:
1766:
GeneReviews/NCBI/NIH/UW entry on
Congenital Disorders of Glycosylation Overview
1248:
Matthijs G, Schollen E, Van
Schaftingen E, Cassiman JJ, Jaeken J (March 1998).
373:
1964:
1780:
1770:
1765:
1486:
2003:
1956:
484:
1455:
1438:
1344:
1327:
1309:
1292:
1689:
1660:
1652:
1623:
1580:
1545:
1494:
1464:
1421:
1383:
1201:
1184:
1153:
1124:
1116:
455:
290:
1414:
10.1002/(SICI)1098-1004(199912)14:6<543::AID-HUMU17>3.0.CO;2-S
1353:
1318:
1283:
1240:
1232:
1210:
1175:
1059:
910:
905:
1527:
953:
747:
728:
30:
1247:
189:
139:
1132:
Jaeken J, Matthijs G (2002). "Congenital disorders of glycosylation".
1051:
80:
76:
1811:
1160:
604:
256:
243:
159:
147:
1036:
1615:
10.1002/1098-1004(200011)16:5<395::AID-HUMU3>3.0.CO;2-T
1572:
10.1002/1098-1004(200011)16:5<386::AID-HUMU2>3.0.CO;2-Y
1509:
1398:
1265:
894:
1667:
1552:
1102:
714:
671:
589:
585:
1595:
1471:
127:
1815:
926:
878:
626:
464:
1697:
1360:
433:
311:
1325:
1217:
1182:
1952:
1944:
1881:
1638:
933:
114:, CDG1, CDG1a, CDGS, PMI, PMI1, PMM 2, phosphomannomutase 2
1436:
1290:
280:
1748:: X-Ray Structure of Human Phosphomannomutase 2 (PMM2)
445:
1437:
Kjaergaard S, Skovby F, Schwartz M (December 1999).
944:
Phosphomannomutase 2 catalyzes the isomerization of
980:
978:
976:
227:
2001:
1810:
973:
18:Protein-coding gene in the species Homo sapiens
1131:
985:GRCm38: Ensembl release 89: ENSMUSG00000022711
1984:
1796:
1713:
1134:Annual Review of Genomics and Human Genetics
1291:Kjaergaard S, Skovby F, Schwartz M (1998).
1991:
1977:
1803:
1789:
1720:
1706:
1030:
1613:
1570:
1535:
1454:
1343:
1308:
1273:
1200:
952:. Mannose 1-phosphate is a precursor to
1085:"Entrez Gene: PMM2 phosphomannomutase 2"
1079:
1077:
2002:
1475:Journal of Inherited Metabolic Disease
404:crypt of lieberkuhn of small intestine
1784:
1701:
1074:
232:
193:
188:
1939:
958:congenital disorder of glycosylation
13:
1443:European Journal of Human Genetics
1332:European Journal of Human Genetics
1297:European Journal of Human Genetics
1254:American Journal of Human Genetics
1095:
14:
2026:
1759:
1641:Molecular Genetics and Metabolism
1376:10.1034/j.1399-0004.1999.550109.x
1105:Molecular Genetics and Metabolism
929:that in humans is encoded by the
1943:
1738:
560:GDP-mannose biosynthetic process
454:
216:
209:
203:
180:
29:
1727:
2015:Human chromosome 16 gene stubs
1012:
994:
570:protein N-linked glycosylation
465:More reference expression data
434:More reference expression data
1:
1682:10.1016/S0378-1119(01)00481-4
1146:10.1146/annurev.genom.2.1.129
966:
201:
1963:. You can help Knowledge by
7:
1516:Journal of Medical Genetics
939:
508:phosphomannomutase activity
10:
2031:
1938:
1894:Phosphoenolpyruvate mutase
1867:Bisphosphoglycerate mutase
1902:
1851:
1843:Precorrin-8X methylmutase
1827:
1733:
1020:"Mouse PubMed Reference:"
1002:"Human PubMed Reference:"
909:
904:
900:
893:
877:
860:
841:
837:
820:
816:
809:
790:
786:
769:
765:
758:
745:
741:
726:
722:
713:
700:
696:
683:
679:
670:
657:
653:
638:
634:
625:
610:
603:
599:
583:
565:mannose metabolic process
483:
479:
462:
453:
444:
431:
380:
371:
318:
309:
279:
271:
267:
250:
237:
200:
179:
170:
166:
121:
118:
108:
101:
96:
73:
68:
51:
46:
41:
37:
28:
23:
1928:Methylmalonyl-CoA mutase
1221:Human Molecular Genetics
1164:Human Molecular Genetics
1862:Phosphoglycerate mutase
1838:Lysolecithin acylmutase
1487:10.1023/A:1005669900330
1456:10.1038/sj.ejhg.5200398
1345:10.1038/sj.ejhg.5200234
1310:10.1038/sj.ejhg.5200194
575:protein targeting to ER
1653:10.1006/mgme.2001.3174
1202:10.1006/geno.1996.4536
1117:10.1006/mgme.1999.2914
871:Chr 16: 8.46 – 8.48 Mb
1913:Cycloartenol synthase
555:protein glycosylation
195:Chromosome 16 (mouse)
1528:10.1136/jmg.37.8.579
923:Phosphomannomutase 2
69:List of PDB id codes
42:Available structures
1918:Lanosterol synthase
1233:10.1093/hmg/7.2.157
950:mannose 1-phosphate
946:mannose 6-phosphate
354:right lobe of liver
1951:This article on a
1877:Phosphomannomutase
1872:Phosphoglucomutase
703:ENSMUSG00000022711
548:Biological process
529:neuronal cell body
517:Cellular component
498:isomerase activity
491:Molecular function
1972:
1971:
1936:
1935:
1756:
1755:
1364:Clinical Genetics
1052:10.1038/ng0597-88
920:
919:
916:
915:
889:
888:
856:
855:
831:
830:
805:
804:
780:
779:
754:
753:
735:
734:
709:
708:
690:
689:
666:
665:
647:
646:
595:
594:
475:
474:
471:
470:
440:
439:
427:
426:
365:
364:
334:bone marrow cells
263:
262:
92:
91:
88:
87:
52:Ortholog search:
2022:
1993:
1986:
1979:
1947:
1940:
1805:
1798:
1791:
1782:
1781:
1742:
1722:
1715:
1708:
1699:
1698:
1693:
1664:
1635:
1617:
1592:
1574:
1549:
1539:
1506:
1468:
1458:
1433:
1395:
1357:
1347:
1322:
1312:
1287:
1277:
1244:
1214:
1204:
1179:
1157:
1128:
1089:
1088:
1081:
1072:
1071:
1034:
1028:
1027:
1016:
1010:
1009:
998:
992:
982:
902:
901:
873:
866:
851:
835:
834:
826:
814:
813:
810:RefSeq (protein)
800:
784:
783:
775:
763:
762:
739:
738:
720:
719:
694:
693:
677:
676:
651:
650:
632:
631:
601:
600:
481:
480:
467:
458:
451:
450:
436:
384:seminal vesicula
376:
374:Top expressed in
369:
368:
322:body of pancreas
314:
312:Top expressed in
307:
306:
286:
285:
269:
268:
259:
246:
235:
220:
213:
207:
196:
184:
168:
167:
162:
160:PMM2 - orthologs
113:
106:
83:
66:
65:
60:
39:
38:
33:
21:
20:
2030:
2029:
2025:
2024:
2023:
2021:
2020:
2019:
2000:
1999:
1998:
1997:
1937:
1932:
1923:Lupeol synthase
1898:
1847:
1823:
1809:
1762:
1757:
1752:
1749:
1743:
1729:
1726:
1696:
1170:(11): 2037–42.
1098:
1096:Further reading
1093:
1092:
1083:
1082:
1075:
1040:Nature Genetics
1035:
1031:
1018:
1017:
1013:
1000:
999:
995:
983:
974:
969:
961:PMM2 deficiency
942:
911:View/Edit Mouse
906:View/Edit Human
869:
864:
861:Location (UCSC)
847:
843:
822:
796:
792:
771:
579:
543:
512:
503:protein binding
463:
432:
423:
418:
414:
410:
406:
402:
398:
394:
390:
386:
372:
361:
356:
352:
348:
344:
340:
336:
332:
328:
326:Achilles tendon
324:
310:
254:
241:
233:
223:
222:
221:
214:
194:
171:Gene location (
122:
109:
102:
75:
53:
19:
12:
11:
5:
2028:
2018:
2017:
2012:
1996:
1995:
1988:
1981:
1973:
1970:
1969:
1948:
1934:
1933:
1931:
1930:
1925:
1920:
1915:
1909:
1907:
1900:
1899:
1897:
1896:
1891:
1890:
1889:
1884:
1874:
1869:
1864:
1858:
1856:
1855:Phosphomutases
1849:
1848:
1846:
1845:
1840:
1834:
1832:
1825:
1824:
1808:
1807:
1800:
1793:
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1760:External links
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1636:
1608:(5): 395–400.
1602:Human Mutation
1593:
1559:Human Mutation
1550:
1507:
1469:
1434:
1402:Human Mutation
1396:
1358:
1323:
1288:
1266:10.1086/301763
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416:pyloric antrum
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396:salivary gland
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273:RNA expression
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17:
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4:
3:
2:
2027:
2016:
2013:
2011:
2008:
2007:
2005:
1994:
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1980:
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1958:
1957:chromosome 16
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1941:
1929:
1926:
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1911:
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1857:
1854:
1850:
1844:
1841:
1839:
1836:
1835:
1833:
1830:
1826:
1821:
1817:
1813:
1806:
1801:
1799:
1794:
1792:
1787:
1786:
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1777:
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1772:
1769:
1767:
1764:
1763:
1747:
1741:
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1735:
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1723:
1718:
1716:
1711:
1709:
1704:
1703:
1700:
1691:
1687:
1683:
1679:
1676:(1–2): 53–9.
1675:
1671:
1666:
1662:
1658:
1654:
1650:
1646:
1642:
1637:
1633:
1629:
1625:
1621:
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1611:
1607:
1603:
1599:
1594:
1590:
1586:
1582:
1578:
1573:
1568:
1565:(5): 386–94.
1564:
1560:
1556:
1551:
1547:
1543:
1538:
1533:
1529:
1525:
1522:(8): 579–80.
1521:
1517:
1513:
1508:
1504:
1500:
1496:
1492:
1488:
1484:
1481:(2): 162–74.
1480:
1476:
1470:
1466:
1462:
1457:
1452:
1448:
1444:
1440:
1435:
1431:
1427:
1423:
1419:
1415:
1411:
1407:
1403:
1397:
1393:
1389:
1385:
1381:
1377:
1373:
1369:
1365:
1359:
1355:
1351:
1346:
1341:
1338:(6): 603–11.
1337:
1333:
1329:
1324:
1320:
1316:
1311:
1306:
1302:
1298:
1294:
1289:
1285:
1281:
1276:
1271:
1267:
1263:
1260:(3): 542–50.
1259:
1255:
1251:
1246:
1242:
1238:
1234:
1230:
1227:(2): 157–64.
1226:
1222:
1216:
1212:
1208:
1203:
1198:
1194:
1190:
1186:
1181:
1177:
1173:
1169:
1165:
1159:
1155:
1151:
1147:
1143:
1139:
1135:
1130:
1126:
1122:
1118:
1114:
1110:
1106:
1101:
1100:
1086:
1080:
1078:
1069:
1065:
1061:
1057:
1053:
1049:
1045:
1041:
1033:
1025:
1021:
1015:
1007:
1003:
997:
990:
986:
981:
979:
977:
972:
964:
962:
959:
955:
951:
947:
937:
935:
932:
928:
924:
912:
907:
903:
899:
896:
892:
885:
883:
880:
876:
872:
868:
863:
859:
852:
850:
846:
840:
836:
833:
827:
825:
819:
815:
812:
808:
801:
799:
795:
789:
785:
782:
776:
774:
768:
764:
761:
759:RefSeq (mRNA)
757:
750:
749:
744:
740:
737:
731:
730:
725:
721:
718:
716:
712:
705:
704:
699:
695:
692:
686:
682:
678:
675:
673:
669:
662:
661:
656:
652:
649:
643:
642:
637:
633:
630:
628:
624:
621:
618:
616:
613:
609:
606:
602:
598:
591:
587:
582:
576:
573:
571:
568:
566:
563:
561:
558:
556:
553:
552:
550:
547:
546:
540:
537:
535:
532:
530:
527:
525:
522:
521:
519:
516:
515:
509:
506:
504:
501:
499:
496:
495:
493:
490:
489:
486:
485:Gene ontology
482:
478:
466:
461:
457:
452:
449:
447:
443:
435:
430:
419:
415:
411:
408:parotid gland
407:
403:
399:
395:
391:
387:
383:
382:
379:
375:
370:
367:
357:
353:
349:
345:
341:
337:
333:
329:
325:
321:
320:
317:
313:
308:
305:
304:
301:
299:
295:
293:
292:
288:
287:
284:
282:
278:
274:
270:
266:
258:
253:
249:
245:
240:
234:16|16 A1
230:
226:
219:
212:
206:
199:
191:
187:
183:
178:
174:
169:
165:
161:
157:
153:
149:
145:
141:
137:
133:
129:
125:
117:
112:
105:
100:
95:
84:
82:
78:
72:
67:
64:
63:
59:
56:
49:
45:
40:
36:
32:
27:
22:
16:
1965:expanding it
1950:
1906:Other groups
1886:
1745:
1673:
1669:
1644:
1640:
1605:
1601:
1562:
1558:
1519:
1515:
1478:
1474:
1449:(8): 884–8.
1446:
1442:
1408:(6): 543–4.
1405:
1401:
1367:
1363:
1335:
1331:
1303:(4): 331–6.
1300:
1296:
1257:
1253:
1224:
1220:
1192:
1188:
1167:
1163:
1137:
1133:
1111:(2): 220–6.
1108:
1104:
1046:(1): 88–92.
1043:
1039:
1032:
1023:
1014:
1005:
996:
943:
930:
922:
921:
849:NP_001349414
842:
821:
798:NM_001362485
791:
770:
746:
727:
701:
684:
658:
639:
619:
614:
392:spermatocyte
296:
289:
119:External IDs
74:
15:
2010:Human genes
1831:Acyl Groups
1728:PDB gallery
1647:(1): 71–6.
1370:(1): 50–4.
1195:(1): 41–7.
954:GDP-mannose
358:endometrium
338:sural nerve
97:Identifiers
2004:Categories
1140:: 129–51.
991:, May 2017
967:References
300:(ortholog)
255:8,480,331
242:8,455,538
140:HomoloGene
1955:on human
1812:Isomerase
845:NP_058577
824:NP_000294
794:NM_016881
773:NM_000303
605:Orthologs
524:cytoplasm
148:GeneCards
1690:11404002
1661:11350185
1632:46522524
1624:11058896
1589:27783974
1581:11058895
1546:10922383
1503:40450186
1495:10801058
1465:10602363
1430:25561064
1422:10571956
1392:28135672
1384:10066032
1189:Genomics
1154:11701646
1125:10527672
1068:22959423
987:–
940:Function
895:Wikidata
584:Sources:
400:duodenum
388:yolk sac
350:placenta
346:duodenum
1816:mutases
1537:1734666
1354:9887379
1319:9781039
1284:9497260
1275:1376957
1241:9425221
1211:9070917
1176:7874123
1060:9140401
989:Ensembl
715:UniProt
672:Ensembl
611:Species
590:QuickGO
539:cytosol
534:nucleus
412:jejunum
275:pattern
136:1859214
104:Aliases
1904:5.4.99
1688:
1659:
1630:
1622:
1587:
1579:
1544:
1534:
1501:
1493:
1463:
1428:
1420:
1390:
1382:
1352:
1317:
1282:
1272:
1239:
1209:
1174:
1152:
1123:
1066:
1058:
927:enzyme
925:is an
881:search
879:PubMed
748:Q9Z2M7
729:O15305
627:Entrez
446:BioGPS
420:morula
342:thymus
330:rectum
128:601785
1959:is a
1853:5.4.2
1829:5.4.1
1628:S2CID
1585:S2CID
1499:S2CID
1426:S2CID
1388:S2CID
1064:S2CID
660:54128
620:Mouse
615:Human
586:Amigo
298:Mouse
291:Human
238:Start
173:Mouse
1961:stub
1953:gene
1887:PMM2
1882:PMM1
1822:5.4)
1746:2amy
1686:PMID
1670:Gene
1657:PMID
1620:PMID
1577:PMID
1542:PMID
1491:PMID
1461:PMID
1418:PMID
1380:PMID
1350:PMID
1315:PMID
1280:PMID
1237:PMID
1207:PMID
1172:PMID
1150:PMID
1121:PMID
1056:PMID
934:gene
931:PMM2
641:5373
281:Bgee
229:Band
190:Chr.
152:PMM2
124:OMIM
111:PMM2
81:2Q4R
77:2AMY
58:RCSB
55:PDBe
24:PMM2
1678:doi
1674:270
1649:doi
1610:doi
1567:doi
1532:PMC
1524:doi
1483:doi
1451:doi
1410:doi
1372:doi
1340:doi
1305:doi
1270:PMC
1262:doi
1229:doi
1197:doi
1142:doi
1113:doi
1048:doi
948:to
865:n/a
685:n/a
251:End
156:OMA
144:257
132:MGI
48:PDB
2006::
1820:EC
1814::
1684:.
1672:.
1655:.
1645:73
1643:.
1626:.
1618:.
1606:16
1604:.
1600:.
1583:.
1575:.
1563:16
1561:.
1557:.
1540:.
1530:.
1520:37
1518:.
1514:.
1497:.
1489:.
1479:23
1477:.
1459:.
1445:.
1441:.
1424:.
1416:.
1406:14
1404:.
1386:.
1378:.
1368:55
1366:.
1348:.
1334:.
1330:.
1313:.
1299:.
1295:.
1278:.
1268:.
1258:62
1256:.
1252:.
1235:.
1223:.
1205:.
1193:40
1191:.
1187:.
1166:.
1148:.
1136:.
1119:.
1109:68
1107:.
1076:^
1062:.
1054:.
1044:16
1042:.
1022:.
1004:.
975:^
963:.
936:.
588:/
257:bp
244:bp
154:;
150::
146:;
142::
138:;
134::
130:;
126::
79:,
1992:e
1985:t
1978:v
1967:.
1818:(
1804:e
1797:t
1790:v
1721:e
1714:t
1707:v
1692:.
1680::
1663:.
1651::
1634:.
1612::
1591:.
1569::
1548:.
1526::
1505:.
1485::
1467:.
1453::
1447:7
1432:.
1412::
1394:.
1374::
1356:.
1342::
1336:6
1321:.
1307::
1301:6
1286:.
1264::
1243:.
1231::
1225:7
1213:.
1199::
1178:.
1168:3
1156:.
1144::
1138:2
1127:.
1115::
1087:.
1070:.
1050::
1026:.
1008:.
175:)
158::
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