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Alliance of Genome Resources

Alliance of Genome Resources is a gene dataset, which contains curated genome information essential for the understanding of the genetics and genomic basis of human biology, health and disease. All data is retrieved from six major model organism databases and the Gene Ontology including FlyBase, Mouse Genome Database (MGI), Rat Genome Database (RGD), Saccharomyces Genome Database (SGD), WormBase, Zebrafish Information Network (ZFIN), and the GO Consortium. In GlyCosmos, only glycan-related disease information has been extracted from Alliance of Genome Resources.

Source Last Updated
Alliance of Genome Resources July 29, 2024
Displaying entries 51 - 75 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB Evidence Code Names ▲ References
DOID:0110644 long QT syndrome 1 MGI:108083 Mus musculus (house mouse) 16535 Kcnq1
  • MGI:6194238
  • PMID:15498462
DOID:9452 steatotic liver disease MGI:104663 Mus musculus (house mouse) 16846 Lep
  • MGI:6194238
  • PMID:25621497
DOID:11721 glycogen storage disease VII MGI:97548 Mus musculus (house mouse) 18642 Pfkm
  • MGI:6194238
  • PMID:19696889
DOID:0080119 mitochondrial DNA depletion syndrome 1 MGI:1920212 Mus musculus (house mouse) 72962 Tymp
  • MGI:6194238
  • PMID:12077348
DOID:9266 cystinuria MGI:1195264 Mus musculus (house mouse) 20532 Slc3a1
  • MGI:6194238
  • PMID:12923163
  • PMID:19484501
  • PMID:25048459
  • PMID:28165480
DOID:9744 type 1 diabetes mellitus MGI:1346060 Mus musculus (house mouse) 24088 Tlr2
  • MGI:6194238
  • PMID:17707128
DOID:1612 breast cancer MGI:98834 Mus musculus (house mouse) 22059 Trp53
  • MGI:6194238
  • PMID:16166291
DOID:0050559 Fukuyama congenital muscular dystrophy MGI:2179507 Mus musculus (house mouse) 246179 Fktn
  • MGI:6194238
  • PMID:15837576
  • PMID:19017726
  • PMID:22922256
DOID:0060350 adenine phosphoribosyltransferase deficiency MGI:88061 Mus musculus (house mouse) 11821 Aprt
  • MGI:6194238
  • PMID:8643571
  • PMID:8864750
DOID:0111041 glycogen storage disease IXb MGI:97578 Mus musculus (house mouse) 102093 Phkb
  • MGI:6194238
  • PMID:36077341
DOID:0050579 glycogen storage disease XV MGI:1351614 Mus musculus (house mouse) 27357 Gyg1
  • MGI:6194238
  • PMID:33219378
DOID:9273 citrullinemia MGI:1354721 Mus musculus (house mouse) 50799 Slc25a13
  • MGI:6194238
  • PMID:14701727
DOID:9352 type 2 diabetes mellitus MGI:96573 Mus musculus (house mouse) 16334 Ins2
  • MGI:6194238
  • PMID:17911348
DOID:0070216 familial hyperinsulinemic hypoglycemia 3 MGI:1270854 Mus musculus (house mouse) 103988 Gck
  • MGI:6194238
  • PMID:33558985
DOID:0110635 muscular dystrophy-dystroglycanopathy type B5 MGI:2447586 Mus musculus (house mouse) 243853 Fkrp
  • MGI:6194238
  • PMID:20675713
DOID:9352 type 2 diabetes mellitus MGI:104874 Mus musculus (house mouse) 11652 Akt2
  • MGI:6194238
  • PMID:11387480
DOID:8584 Burkitt lymphoma MGI:97250 Mus musculus (house mouse) 17869 Myc
  • MGI:6194238
  • PMID:15687498
DOID:0110170 Charcot-Marie-Tooth disease axonal type 2Q MGI:2445096 Mus musculus (house mouse) 209692 Dhtkd1
  • MGI:6194238
  • PMID:29661920
  • PMID:32169121
DOID:1919 Lesch-Nyhan syndrome MGI:96217 Mus musculus (house mouse) 15452 Hprt1
  • MGI:6194238
  • PMID:11297820
  • PMID:7509865
DOID:0060233 cardiofaciocutaneous syndrome MGI:88190 Mus musculus (house mouse) 109880 Braf
  • MGI:6194238
  • PMID:21383153
  • PMID:25035421
  • PMID:26472072
DOID:13317 hyperinsulinemic hypoglycemia MGI:1270854 Mus musculus (house mouse) 103988 Gck
  • MGI:6194238
  • PMID:17353190
DOID:0050570 congenital disorder of glycosylation type I MGI:97075 Mus musculus (house mouse) 110119 Mpi
  • MGI:6194238
  • PMID:16339137
DOID:14504 Niemann-Pick disease MGI:1097712 Mus musculus (house mouse) 18145 Npc1
  • MGI:6194238
  • PMID:12528192
  • PMID:15071184
  • PMID:18160655
  • PMID:20007718
  • PMID:21303697
  • PMID:21856732
  • PMID:21896731
  • PMID:22048958
  • PMID:22163015
  • PMID:22869680
  • PMID:23843985
  • PMID:24391715
  • PMID:26019327
  • PMID:6257302
  • PMID:7202025
  • PMID:9950794
DOID:13482 Proteus syndrome MGI:87986 Mus musculus (house mouse) 11651 Akt1
  • MGI:6194238
  • PMID:31194862
DOID:0070253 congenital disorder of glycosylation type IIa MGI:2384966 Mus musculus (house mouse) 217664 Mgat2
  • MGI:6194238
  • PMID:11805078

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Supported by JST NBDC Grant Number JPMJND2204

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Last updated: August 19, 2024