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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 October 9, 2024
Displaying entries 71151 - 71175 of 71927 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB Evidence Code Names References ▼
DOID:5844 myocardial infarction HGNC:7176 Homo sapiens (human) 4318 MMP9
  • MGI:6194238
  • PMID:15118287
  • PMID:17893005
DOID:0060639 permanent neonatal diabetes mellitus HGNC:6257 Homo sapiens (human) 3767 KCNJ11
  • MGI:6194238
  • PMID:15115830
  • PMID:16670688
  • RGD:7240710
DOID:10763 hypertension HGNC:12518 Homo sapiens (human) 7351 UCP2
  • MGI:6194238
  • PMID:15106800
DOID:0110875 holoprosencephaly 3 MGI:98297 Mus musculus (house mouse) 20423 Shh
  • MGI:6194238
  • PMID:15105374
  • PMID:8837770
DOID:0111100 maturity-onset diabetes of the young type 2 MGI:1270854 Mus musculus (house mouse) 103988 Gck
  • MGI:6194238
  • PMID:15102714
  • PMID:15161764
  • PMID:15569412
  • PMID:17353190
  • PMID:19952346
  • PMID:24447392
  • PMID:7553875
  • PMID:7665557
  • PMID:8530440
  • PMID:9867845
DOID:8893 psoriasis MGI:103178 Mus musculus (house mouse) 22339 Vegfa
  • MGI:6194238
  • PMID:15100155
DOID:4535 hypotrichosis RGD:735015 Rattus norvegicus (Norway rat) 291754 Dsg4
  • MGI:6194238
  • PMID:15081105
  • PMID:15606503
  • PMID:15617564
DOID:0050741 alcohol dependence RGD:61800 Rattus norvegicus (Norway rat) 29595 Htr2a
  • MGI:6194238
  • PMID:15080502
  • PMID:8822536
DOID:13359 Ehlers-Danlos syndrome HGNC:2198 Homo sapiens (human) 1278 COL1A2
  • MGI:6194238
  • PMID:15077201
DOID:14504 Niemann-Pick disease MGI:1915213 Mus musculus (house mouse) 67963 Npc2
  • MGI:6194238
  • PMID:15071184
  • PMID:23843985
DOID:9970 obesity MGI:97742 Mus musculus (house mouse) 18976 Pomc
  • MGI:6194238
  • PMID:15070780
DOID:12930 dilated cardiomyopathy HGNC:11947 Homo sapiens (human) 7137 TNNI3
  • MGI:6194238
  • PMID:15070570
DOID:0110922 familial hemophagocytic lymphohistiocytosis 2 MGI:97551 Mus musculus (house mouse) 18646 Prf1
  • MGI:6194238
  • PMID:15069016
  • PMID:23160464
DOID:8947 diabetic retinopathy HGNC:8824 Homo sapiens (human) 5176 SERPINF1
  • MGI:6194238
  • PMID:15059706
  • PMID:17658465
  • PMID:18455830
  • PMID:19365032
DOID:13580 cholestasis HGNC:53 Homo sapiens (human) 1244 ABCC2
  • MGI:6194238
  • PMID:15057744
DOID:0110629 Wolfram syndrome 1 MGI:1328355 Mus musculus (house mouse) 22393 Wfs1
  • MGI:6194238
  • PMID:15056606
  • PMID:16215705
  • PMID:18343518
  • PMID:21031341
  • PMID:24710642
  • PMID:37386014
DOID:0090019 sitosterolemia MGI:1914720 Mus musculus (house mouse) 67470 Abcg8
  • MGI:6194238
  • PMID:15040800
DOID:13025 retinopathy of prematurity RGD:2965 Rattus norvegicus (Norway rat) 25589 Kdr
  • MGI:6194238
  • PMID:15039215
  • PMID:30652694
DOID:1612 breast cancer HGNC:3467 Homo sapiens (human) 2099 ESR1
  • MGI:6194238
  • PMID:15034868
  • PMID:15604249
  • PMID:17553133
  • PMID:19011961
  • PMID:19320640
  • PMID:19636371
  • PMID:20846920
  • RGD:7240710
DOID:2921 glomerulonephritis HGNC:7173 Homo sapiens (human) 4314 MMP3
  • MGI:6194238
  • PMID:15034162
DOID:10581 metachromatic leukodystrophy HGNC:713 Homo sapiens (human) 410 ARSA
  • MGI:6194238
  • PMID:15026521
  • PMID:15375602
  • RGD:7240710
DOID:1270 hereditary hemorrhagic telangiectasia HGNC:175 Homo sapiens (human) 94 ACVRL1
  • MGI:6194238
  • PMID:15024723
  • PMID:16752392
  • PMID:17219009
  • PMID:18543223
  • RGD:7240710
DOID:5844 myocardial infarction HGNC:7155 Homo sapiens (human) 4312 MMP1
  • MGI:6194238
  • PMID:15009768
  • PMID:16210545
  • PMID:19797822
DOID:0111809 syndromic microphthalmia 2 HGNC:20893 Homo sapiens (human) 54880 BCOR
  • MGI:6194238
  • PMID:15004558
  • RGD:7240710
DOID:0110320 hypertrophic cardiomyopathy 14 MGI:97255 Mus musculus (house mouse) 17888 Myh6
  • MGI:6194238
  • PMID:15001446
  • PMID:16332958
  • PMID:20811150
  • PMID:24829265
  • PMID:8614836

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Last updated: December 9, 2024