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that blocks aerobic glycolysis by preventing the transport of pyruvate from the cytosol into the mitochondrion for oxidative phosphorylation; however, anaerobic glycolysis is preserved. Common signs and symptoms include poor growth, normal lactate/pyruvate ratio (however both lactate and pyruvate are
1664:
in higher than normal concentrations), hepatomegaly, lactic acidosis, hypoglycemia, neurological problems, and hypotonia. A disease with comparable symptoms is also seen in autosomal recessive mutations of the MPC2 gene.
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1601:
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Mitochondrial pyruvate carrier deficiency (MPYCD) is an autosomal recessive disease due to mutations in the MPC1 gene on chromosome 6q27. It is an
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1826:"MPC2 variants disrupt mitochondrial pyruvate metabolism and cause an early-onset mitochondriopathy"
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1959:
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Pujol C, Lebigot E, Gaignard P, Galai S, Kraoua I, Bault JP, et al. (March 2023).
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National Center for
Biotechnology Information, U.S. National Library of Medicine
1745:
National Center for
Biotechnology Information, U.S. National Library of Medicine
421:
2684:
2563:
2400:
2260:
1048:
Click on genes, proteins and metabolites below to link to respective articles.
237:
134:
84:
59:, BRP44L, MPYCD, dJ68L15.3, CGI-129, mitochondrial pyruvate carrier 1, SLC54A1
2059:
1841:
643:
481:
359:
304:
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2009:
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17:
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2975:
2937:
2932:
2304:
1800:
1016:
72:
2426:
1873:
1524:
1062:
2225:(Pompe's disease, glucosidase deficiency, formerly GSD-IIa)
1640:
The interactive pathway map can be edited at WikiPathways:
599:
mitochondrial acetyl-CoA biosynthetic process from pyruvate
2336:(von Gierke's disease, glucose 6-phosphatase deficiency)
2181:(Hers' disease, liver glycogen phosphorylase deficiency)
328:
2987:
493:
2405:
Fatal congenital nonlysosomal cardiac glycogenosis (
2924:
2805:
2695:
2465:
2381:
2347:
2314:
2259:
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2163:
2154:
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1958:
1934:
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910:
865:
831:
806:
1719:
1717:
1715:
1698:
1696:
1694:
578:integral component of mitochondrial inner membrane
2280:(Tarui's disease, phosphofructokinase deficiency)
2130:(Andersen's disease, branching enzyme deficiency)
275:
174:
2187:(McArdle's disease, myophosphorylase deficiency)
2175:(Cori's disease, debranching enzyme deficiency)
1528:
1066:
609:cellular response to leukemia inhibitory factor
27:Protein-coding gene in the species Homo sapiens
1724:GRCm38: Ensembl release 89: ENSMUSG00000023861
604:mitochondrial pyruvate transmembrane transport
3007:
2438:
1885:
8:
2357:Glucose-6-phosphate dehydrogenase deficiency
2373:6-phosphogluconate dehydrogenase deficiency
1703:GRCh38: Ensembl release 89: ENSG00000060762
1027:. This protein is involved in transport of
537:pyruvate transmembrane transporter activity
3014:
3000:
2445:
2431:
2423:
2256:
2160:
2109:
2028:
2018:
1931:
1892:
1878:
1870:
1805:Online Mendelian Inheritance in Man (OMIM)
862:
639:
519:
316:
215:
112:
2938:Mitochondrial pyruvate carrier deficiency
2305:Mitochondrial pyruvate carrier deficiency
1849:
3043:Inborn errors of carbohydrate metabolism
1974:Inborn errors of renal tubular transport
1801:"Mitochondrial pyruvate carrier 1; MPC1"
1679:Inborn errors of carbohydrate metabolism
2833:Recessive multiple epiphyseal dysplasia
2596:Congenital endothelial dystrophy type 2
1690:
1661:inborn error of carbohydrate metabolism
1633:
29:
1611:|alt=Glycolysis and Gluconeogenesis
280:
241:
236:
179:
138:
133:
7:
2964:
2962:
2284:Triosephosphate isomerase deficiency
2231:(LAMP2 deficiency, formerly GSD-IIb)
2298:Phosphoglucose isomerase deficiency
2199:(PGM1-CDG, CDG1T, formerly GSD-XIV)
2986:. You can help Knowledge (XXG) by
2329:Fructose bisphosphatase deficiency
2301:Phosphoglycerate kinase deficiency
907:
828:
803:
779:
760:
734:
715:
689:
670:
498:
416:
354:
333:
25:
2193:(phosphorylase kinase deficiency)
1643:"GlycolysisGluconeogenesis_WP534"
1012:that in humans is encoded by the
2966:
2643:Thyroid dyshormonogenesis type 1
2223:Glycogen storage disease type II
1781:HUGO Gene Nomenclature Committee
1674:Mitochondrial pyruvate carrier 2
1624:Glycolysis and Gluconeogenesis
1002:Mitochondrial pyruvate carrier 1
264:
257:
251:
228:
163:
156:
150:
125:
2820:Multiple epiphyseal dysplasia 4
2615:Glucose-galactose malabsorption
2324:Pyruvate carboxylase deficiency
2134:Adult polyglucosan body disease
1969:Glucose-galactose malabsorption
1037:pyruvate dehydrogenase reaction
2124:(glycogen synthase deficiency)
1021:Mitochondrial Pyruvate Carrier
558:integral component of membrane
482:More reference expression data
1:
3048:Autosomal recessive disorders
3038:Human chromosome 6 gene stubs
2752:Allan–Herndon–Dudley syndrome
2671:Lysinuric protein intolerance
2197:Phosphoglucomutase deficiency
1031:across the inner membrane of
249:
148:
2900:Acrodermatitis enteropathica
2550:Arterial tortuosity syndrome
2407:AMP-activated protein kinase
563:mitochondrial inner membrane
3033:Genes on human chromosome 6
2582:Hereditary elliptocytosis 4
1008:(BRP44L) and SLC54A1, is a
3074:
2961:
2578:Hereditary spherocytosis 4
2369:(Transketolase deficiency)
2289:Pyruvate kinase deficiency
2947:
2838:Atelosteogenesis, type II
2349:Pentose phosphate pathway
1915:glycogen storage diseases
1759:"Mouse PubMed Reference:"
1741:"Human PubMed Reference:"
988:
983:
979:
972:
956:
943:Chr 6: 166.36 – 166.38 Mb
937:
914:
889:
858:
835:
810:
799:
786:
782:
767:
763:
754:
741:
737:
722:
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696:
692:
677:
673:
664:
649:
642:
638:
622:
522:
518:
506:
501:
492:
479:
440:quadriceps femoris muscle
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:
2362:Transaldolase deficiency
2522:Fanconi-Bickel syndrome
2147:(glycogenin deficiency)
1995:Fanconi-Bickel syndrome
1905:carbohydrate metabolism
1043:Interactive pathway map
1035:in preparation for the
2536:Fructose malabsorption
1984:Fructose malabsorption
1605:
1143:
1004:(MPC1), also known as
456:skeletal muscle tissue
3058:Solute carrier family
2952:solute carrier family
2914:African iron overload
2843:Diastrophic dysplasia
2394:Primary hyperoxaluria
2294:Aldolase A deficiency
2044:Essential fructosuria
1911:metabolism disorders
1842:10.1093/brain/awac444
1655:Clinical significance
1604:
1142:
1006:brain protein 44-like
950:Chr 17: 8.5 – 8.52 Mb
282:17 A1|17 4.92 cM
243:Chromosome 17 (mouse)
2885:Von Gierke's disease
2766:Von Gierke's disease
2049:Fructose intolerance
1945:Congenital alactasia
1777:"HGNC data for MPC1"
1019:. It is part of the
444:white adipose tissue
141:Chromosome 6 (human)
1950:Sucrose intolerance
390:right lobe of liver
3053:Transport proteins
2974:This article on a
2601:Fuchs' dystrophy 4
1997:(GLUT2 deficiency)
1991:(GLUT1 deficiency)
1606:
1144:
744:ENSMUSG00000023861
614:biological process
592:Biological process
583:cellular component
551:Cellular component
542:molecular function
530:Molecular function
2995:
2994:
2959:
2958:
2724:Gitelman syndrome
2480:Episodic ataxia 6
2420:
2419:
2343:
2342:
2307:(MPC1 deficiency)
2242:
2241:
2238:
2237:
2095:
2094:
2091:
2090:
2004:
2003:
999:
998:
995:
994:
968:
967:
933:
932:
904:
903:
854:
853:
825:
824:
795:
794:
776:
775:
750:
749:
731:
730:
705:
704:
686:
685:
634:
633:
514:
513:
510:
509:
488:
487:
475:
474:
464:cerebellar cortex
413:
412:
311:
310:
210:
209:
16:(Redirected from
3065:
3016:
3009:
3002:
2970:
2963:
2857:Pendred syndrome
2629:Renal glycosuria
2454:Genetic disorder
2447:
2440:
2433:
2424:
2257:
2216:
2166:
2161:
2110:
2067:
2037:
2029:
2019:
1978:Renal glycosuria
1932:
1894:
1887:
1880:
1871:
1864:
1863:
1853:
1821:
1815:
1814:
1812:
1811:
1797:
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1787:
1773:
1767:
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1755:
1749:
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1737:
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899:
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859:RefSeq (protein)
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804:
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761:
735:
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671:
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484:
424:
422:Top expressed in
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360:Top expressed in
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255:
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216:
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105:MPC1 - orthologs
58:
51:
30:
21:
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3062:
3023:
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2955:
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2920:
2825:Achondrogenesis
2801:
2710:Crohn's disease
2691:
2657:Hartnup disease
2508:De Vivo disease
2461:
2451:
2421:
2416:
2377:
2339:
2316:Gluconeogenesis
2310:
2234:
2207:
2202:
2165:Extralysosomal:
2164:
2150:
2087:
2083:GALE deficiency
2079:GALT deficiency
2074:GALK deficiency
2058:
2053:
2032:
2000:
1989:De Vivo Disease
1954:
1928:(extracellular)
1927:
1918:
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1898:
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1368:
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1201:
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1148:
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1045:
990:View/Edit Mouse
985:View/Edit Human
948:
941:
938:Location (UCSC)
924:
920:
916:
895:
891:
885:
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873:
869:
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816:
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725:ENSG00000060762
618:
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448:muscle of thigh
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432:proximal tubule
420:
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394:muscle of thigh
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372:
370:right ventricle
358:
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219:Gene location (
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161:
139:
116:Gene location (
67:
54:
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28:
23:
22:
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2598:
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2554:
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2512:
2511:
2510:
2498:
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2482:
2469:
2467:
2463:
2462:
2458:Solute carrier
2452:
2450:
2449:
2442:
2435:
2427:
2418:
2417:
2415:
2414:
2403:
2398:
2397:
2396:
2385:
2383:
2379:
2378:
2376:
2375:
2370:
2364:
2359:
2353:
2351:
2345:
2344:
2341:
2340:
2338:
2337:
2331:
2326:
2320:
2318:
2312:
2311:
2309:
2308:
2302:
2299:
2296:
2291:
2286:
2281:
2275:
2265:
2263:
2254:
2244:
2243:
2240:
2239:
2236:
2235:
2233:
2232:
2226:
2219:
2217:
2204:
2203:
2201:
2200:
2194:
2188:
2182:
2176:
2169:
2167:
2158:
2156:Glycogenolysis
2152:
2151:
2149:
2148:
2142:
2140:Lafora disease
2137:
2131:
2125:
2118:
2116:
2107:
2097:
2096:
2093:
2092:
2089:
2088:
2086:
2085:
2076:
2070:
2068:
2055:
2054:
2052:
2051:
2046:
2040:
2038:
2026:
2023:Monosaccharide
2016:
2006:
2005:
2002:
2001:
1999:
1998:
1992:
1986:
1981:
1971:
1965:
1963:
1960:Monosaccharide
1956:
1955:
1953:
1952:
1947:
1941:
1939:
1929:
1920:
1919:
1909:monosaccharide
1899:
1897:
1896:
1889:
1882:
1874:
1866:
1865:
1836:(3): 858–864.
1816:
1792:
1768:
1750:
1732:
1711:
1689:
1688:
1686:
1683:
1682:
1681:
1676:
1669:
1666:
1656:
1653:
1649:
1648:
1632:
1631:
1620:
1619:
1523:
1517:
1512:
1507:
1502:
1497:
1492:
1487:
1482:
1477:
1472:
1467:
1462:
1457:
1452:
1447:
1442:
1437:
1432:
1427:
1422:
1417:
1412:
1407:
1402:
1397:
1392:
1387:
1382:
1377:
1372:
1367:
1362:
1357:
1352:
1347:
1342:
1337:
1332:
1327:
1322:
1317:
1312:
1307:
1302:
1297:
1292:
1287:
1282:
1277:
1272:
1267:
1262:
1257:
1252:
1247:
1242:
1237:
1232:
1227:
1222:
1217:
1212:
1207:
1202:
1197:
1192:
1187:
1182:
1177:
1172:
1167:
1162:
1157:
1152:
1147:
1146:
1061:
1060:
1059:
1058:
1056:
1055:
1054:
1053:
1052:
1051:
1044:
1041:
1025:protein family
997:
996:
993:
992:
987:
977:
976:
970:
969:
966:
965:
963:
961:
954:
953:
946:
939:
935:
934:
931:
930:
912:
911:
905:
902:
901:
887:
886:
860:
856:
855:
852:
851:
833:
832:
826:
823:
822:
808:
807:
801:
797:
796:
793:
792:
784:
783:
777:
774:
773:
765:
764:
758:
752:
751:
748:
747:
739:
738:
732:
729:
728:
720:
719:
713:
707:
706:
703:
702:
694:
693:
687:
684:
683:
675:
674:
668:
662:
661:
656:
651:
647:
646:
636:
635:
632:
631:
620:
619:
617:
616:
611:
606:
601:
595:
593:
589:
588:
586:
585:
580:
575:
570:
565:
560:
554:
552:
548:
547:
545:
544:
539:
533:
531:
527:
526:
516:
515:
512:
511:
508:
507:
504:
503:
496:
490:
489:
486:
485:
477:
476:
473:
472:
470:
469:
465:
461:
457:
453:
449:
445:
441:
437:
433:
429:
426:
425:
414:
411:
410:
408:
407:
403:
399:
395:
391:
387:
383:
379:
375:
374:left ventricle
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:
24:
14:
13:
10:
9:
6:
4:
3:
2:
3070:
3059:
3056:
3054:
3051:
3049:
3046:
3044:
3041:
3039:
3036:
3034:
3031:
3030:
3028:
3017:
3012:
3010:
3005:
3003:
2998:
2997:
2991:
2989:
2985:
2981:
2977:
2972:
2969:
2965:
2954:
2953:
2946:
2939:
2935:
2934:
2930:
2929:
2927:
2923:
2915:
2912:
2911:
2910:
2909:
2905:
2901:
2898:
2897:
2896:
2895:
2891:
2886:
2883:
2882:
2881:
2880:
2876:
2872:
2869:
2868:
2867:
2866:
2862:
2858:
2855:
2854:
2853:
2852:
2848:
2844:
2841:
2839:
2836:
2834:
2831:
2829:
2826:
2823:
2821:
2818:
2817:
2816:
2815:
2811:
2810:
2808:
2804:
2796:
2793:
2792:
2791:
2790:
2786:
2782:
2781:Salla disease
2779:
2778:
2777:
2776:
2772:
2767:
2764:
2763:
2762:
2761:
2757:
2753:
2750:
2749:
2748:
2747:
2743:
2739:
2736:
2735:
2734:
2733:
2729:
2725:
2722:
2721:
2720:
2719:
2715:
2711:
2708:
2707:
2706:
2705:
2701:
2700:
2698:
2694:
2686:
2683:
2682:
2681:
2680:
2676:
2672:
2669:
2668:
2667:
2666:
2662:
2658:
2655:
2654:
2653:
2652:
2648:
2644:
2641:
2640:
2639:
2638:
2634:
2630:
2627:
2626:
2625:
2624:
2620:
2616:
2613:
2612:
2611:
2610:
2606:
2602:
2599:
2597:
2594:
2593:
2592:
2591:
2587:
2583:
2579:
2576:
2575:
2574:
2573:
2569:
2565:
2562:
2561:
2560:
2559:
2555:
2551:
2548:
2547:
2546:
2545:
2541:
2537:
2534:
2533:
2532:
2531:
2527:
2523:
2520:
2519:
2518:
2517:
2513:
2509:
2506:
2505:
2504:
2503:
2499:
2495:
2492:
2491:
2490:
2489:
2485:
2481:
2478:
2477:
2476:
2475:
2471:
2470:
2468:
2464:
2459:
2455:
2448:
2443:
2441:
2436:
2434:
2429:
2428:
2425:
2412:
2408:
2404:
2402:
2399:
2395:
2392:
2391:
2390:
2389:Hyperoxaluria
2387:
2386:
2384:
2380:
2374:
2371:
2368:
2365:
2363:
2360:
2358:
2355:
2354:
2352:
2350:
2346:
2335:
2332:
2330:
2327:
2325:
2322:
2321:
2319:
2317:
2313:
2306:
2303:
2300:
2297:
2295:
2292:
2290:
2287:
2285:
2282:
2279:
2276:
2274:
2270:
2267:
2266:
2264:
2262:
2258:
2255:
2253:
2249:
2245:
2230:
2229:Danon disease
2227:
2224:
2221:
2220:
2218:
2214:
2210:
2205:
2198:
2195:
2192:
2189:
2186:
2183:
2180:
2177:
2174:
2171:
2170:
2168:
2162:
2159:
2157:
2153:
2146:
2143:
2141:
2138:
2135:
2132:
2129:
2126:
2123:
2120:
2119:
2117:
2115:
2111:
2108:
2106:
2102:
2098:
2084:
2080:
2077:
2075:
2072:
2071:
2069:
2065:
2061:
2056:
2050:
2047:
2045:
2042:
2041:
2039:
2035:
2030:
2027:
2024:
2020:
2017:
2015:
2011:
2007:
1996:
1993:
1990:
1987:
1985:
1982:
1979:
1975:
1972:
1970:
1967:
1966:
1964:
1961:
1957:
1951:
1948:
1946:
1943:
1942:
1940:
1937:
1933:
1930:
1925:
1921:
1916:
1910:
1906:
1902:
1895:
1890:
1888:
1883:
1881:
1876:
1875:
1872:
1861:
1857:
1852:
1847:
1843:
1839:
1835:
1831:
1827:
1820:
1817:
1806:
1802:
1796:
1793:
1782:
1778:
1772:
1769:
1764:
1760:
1754:
1751:
1746:
1742:
1736:
1733:
1729:
1725:
1720:
1718:
1716:
1712:
1708:
1704:
1699:
1697:
1695:
1691:
1684:
1680:
1677:
1675:
1672:
1671:
1667:
1665:
1662:
1654:
1644:
1637:
1634:
1627:
1622:
1614:
1527:
1065:
1050:
1049:
1042:
1040:
1038:
1034:
1030:
1026:
1022:
1018:
1015:
1011:
1007:
1003:
991:
986:
982:
978:
975:
971:
964:
962:
959:
955:
951:
947:
944:
940:
936:
929:
927:
923:
919:
913:
909:
906:
900:
898:
894:
888:
884:
880:
876:
872:
868:
864:
861:
857:
850:
848:
844:
840:
834:
830:
827:
821:
819:
815:
809:
805:
802:
800:RefSeq (mRNA)
798:
791:
790:
785:
781:
778:
772:
771:
766:
762:
759:
757:
753:
746:
745:
740:
736:
733:
727:
726:
721:
717:
714:
712:
708:
701:
700:
695:
691:
688:
682:
681:
676:
672:
669:
667:
663:
660:
657:
655:
652:
648:
645:
641:
637:
630:
626:
621:
615:
612:
610:
607:
605:
602:
600:
597:
596:
594:
591:
590:
584:
581:
579:
576:
574:
573:mitochondrion
571:
569:
566:
564:
561:
559:
556:
555:
553:
550:
549:
543:
540:
538:
535:
534:
532:
529:
528:
525:
524:Gene ontology
521:
517:
505:
500:
497:
495:
491:
483:
478:
467:
463:
459:
455:
452:muscle tissue
451:
447:
443:
439:
435:
431:
430:
427:
423:
418:
415:
405:
402:parotid gland
401:
397:
393:
389:
385:
382:apex of heart
381:
378:right auricle
377:
373:
369:
368:
365:
361:
356:
353:
352:
349:
347:
343:
341:
340:
336:
335:
332:
330:
326:
322:
318:
314:
306:
301:
297:
293:
288:
278:
274:
267:
260:
254:
247:
239:
235:
231:
226:
222:
217:
213:
205:
200:
196:
192:
187:
177:
173:
166:
159:
153:
146:
142:
136:
132:
128:
123:
119:
114:
110:
106:
102:
98:
94:
90:
86:
82:
78:
74:
70:
62:
57:
50:
45:
40:
36:
31:
19:
2988:expanding it
2980:chromosome 6
2973:
2949:
2931:
2906:
2892:
2877:
2863:
2849:
2812:
2787:
2773:
2758:
2744:
2730:
2716:
2702:
2677:
2663:
2649:
2635:
2621:
2607:
2588:
2570:
2556:
2542:
2528:
2514:
2500:
2486:
2472:
2456:, membrane:
2409:deficiency,
2278:GSD type VII
2173:GSD type III
2114:Glycogenesis
2064:galactosemia
1936:Disaccharide
1901:Inborn error
1833:
1829:
1819:
1808:. Retrieved
1804:
1795:
1784:. Retrieved
1780:
1771:
1762:
1753:
1744:
1735:
1658:
1636:
1047:
1046:
1033:mitochondria
1013:
1005:
1001:
1000:
926:NP_001351848
922:NP_001351847
915:
897:NP_001363498
893:NP_001363497
890:
883:NP_001363496
879:NP_001363495
875:NP_001363494
867:NP_001257808
847:NM_001364919
843:NM_001364918
836:
814:NM_001270879
811:
787:
768:
742:
723:
697:
678:
658:
653:
460:human kidney
436:right kidney
398:human kidney
344:
337:
202:166,383,013
189:166,364,919
64:External IDs
2191:GSD type IX
2179:GSD type VI
2145:GSD type XV
2128:GSD type IV
1926:, transport
42:Identifiers
3027:Categories
2685:Cystinuria
2564:Cystinuria
2401:Pentosuria
2334:GSD type I
2261:Glycolysis
2185:GSD type V
2122:GSD type 0
2025:catabolism
1938:catabolism
1913:Including
1810:2023-08-21
1786:2023-08-21
1730:, May 2017
1709:, May 2017
1685:References
406:myocardium
386:C1 segment
348:(ortholog)
303:8,516,493
290:8,501,736
85:HomoloGene
2978:on human
2950:see also
2460:disorders
2209:Lysosomal
2060:Galactose
1962:transport
918:NP_061289
871:NP_057182
839:NM_018819
818:NM_016098
644:Orthologs
93:GeneCards
2887:, GSD-Ib
2768:, GSD-Ic
2105:glycogen
2034:Fructose
1860:36417180
1726:–
1705:–
1668:See also
1029:pyruvate
974:Wikidata
623:Sources:
568:membrane
2933:SLC54A1
2908:SLC40A1
2894:SLC39A4
2879:SLC37A4
2871:CDOG 2C
2865:SLC35C1
2851:SLC26A4
2828:type 1B
2814:SLC26A2
2789:SLC17A8
2775:SLC17A5
2760:SLC17A3
2746:SLC16A2
2732:SLC16A1
2718:SLC12A3
2704:SLC11A1
2651:SLC6A19
2590:SLC4A11
2544:SLC2A10
2494:SPATCCM
2248:Glucose
2101:Glucose
2014:glucose
1924:Sucrose
1851:9976959
1728:Ensembl
1707:Ensembl
1057:[[File:
1010:protein
756:UniProt
711:Ensembl
650:Species
629:QuickGO
323:pattern
81:1915240
49:Aliases
2795:DFNA25
2679:SLC7A9
2665:SLC7A7
2637:SLC5A5
2623:SLC5A2
2609:SLC5A1
2572:SLC4A1
2558:SLC3A1
2530:SLC2A5
2516:SLC2A2
2502:SLC2A1
2488:SLC1A4
2474:SLC1A3
2411:PRKAG2
2269:MODY 2
2136:(APBD)
2010:Hexose
1858:
1848:
1023:(MPC)
960:search
958:PubMed
789:P63030
770:Q9Y5U8
666:Entrez
494:BioGPS
73:614738
2982:is a
2925:51-60
2806:21-40
2696:11-20
2382:Other
2367:SDDHD
1917:(GSD)
1830:Brain
699:55951
680:51660
659:Mouse
654:Human
625:Amigo
468:heart
346:Mouse
339:Human
286:Start
221:Mouse
185:Start
118:Human
2984:stub
2976:gene
2738:HHF7
2466:1-10
2273:HHF3
1856:PMID
1626:edit
1613:edit
1017:gene
1014:MPC1
329:Bgee
277:Band
238:Chr.
181:6q27
176:Band
135:Chr.
97:MPC1
89:9384
69:OMIM
56:MPC1
33:MPC1
18:MPC1
2252:CAC
2213:LSD
1903:of
1846:PMC
1838:doi
1834:146
502:n/a
299:End
198:End
101:OMA
77:MGI
3029::
2250:⇄
2215:):
2103:⇄
2062:/
2012:→
1907::
1854:.
1844:.
1832:.
1828:.
1803:.
1779:.
1761:.
1743:.
1714:^
1693:^
1615:]]
1039:.
627:/
305:bp
292:bp
204:bp
191:bp
99:;
95::
91:;
87::
83:;
79::
75:;
71::
3015:e
3008:t
3001:v
2990:.
2940:)
2936:(
2580:/
2446:e
2439:t
2432:v
2413:)
2271:/
2211:(
2081:/
2066::
2036::
1980:)
1976:(
1893:e
1886:t
1879:v
1862:.
1840::
1813:.
1789:.
1765:.
1747:.
1645:.
1519:]
1514:]
1509:]
1504:]
1499:]
1494:]
1489:]
1484:]
1479:]
1474:]
1469:]
1464:]
1459:]
1454:]
1449:]
1444:]
1439:]
1434:]
1429:]
1424:]
1419:]
1414:]
1409:]
1404:]
1399:]
1394:]
1389:]
1384:]
1379:]
1374:]
1369:]
1364:]
1359:]
1354:]
1349:]
1344:]
1339:]
1334:]
1329:]
1324:]
1319:]
1314:]
1309:]
1304:]
1299:]
1294:]
1289:]
1284:]
1279:]
1274:]
1269:]
1264:]
1259:]
1254:]
1249:]
1244:]
1239:]
1234:]
1229:]
1224:]
1219:]
1214:]
1209:]
1204:]
1199:]
1194:]
1189:]
1184:]
1179:]
1174:]
1169:]
1164:]
1159:]
1154:]
1149:]
223:)
120:)
103::
20:)
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