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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 69751 - 69775 of 71927 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB Evidence Code Names References ▼
DOID:6000 congestive heart failure RGD:2802 Rattus norvegicus (Norway rat) 25459 Hmgb1
  • MGI:6194238
  • PMID:24204700
DOID:5844 myocardial infarction HGNC:7997 Homo sapiens (human) 3084 NRG1
  • MGI:6194238
  • PMID:24200746
  • PMID:27993643
DOID:0080208 metabolic dysfunction-associated steatotic liver disease RGD:620329 Rattus norvegicus (Norway rat) 252900 Dgat2
  • MGI:6194238
  • PMID:24166662
  • PMID:26394137
DOID:4928 intrahepatic cholangiocarcinoma HGNC:6407 Homo sapiens (human) 3845 KRAS
  • MGI:6194238
  • PMID:24139215
DOID:684 hepatocellular carcinoma HGNC:12363 Homo sapiens (human) 7249 TSC2
  • MGI:6194238
  • PMID:24119083
DOID:6364 migraine HGNC:1388 Homo sapiens (human) 773 CACNA1A
  • MGI:6194238
  • PMID:24108129
DOID:418 systemic scleroderma MGI:95489 Mus musculus (house mouse) 14118 Fbn1
  • MGI:6194238
  • PMID:24107997
DOID:14503 neuronal ceroid lipofuscinosis FB:FBgn0030057 Drosophila melanogaster (fruit fly) 31805 Ppt1
  • MGI:6194238
  • PMID:24091420
DOID:0050431 arrhythmogenic right ventricular cardiomyopathy HGNC:3049 Homo sapiens (human) 1829 DSG2
  • MGI:6194238
  • PMID:24086444
  • PMID:30239670
  • PMID:30304392
  • PMID:30454721
DOID:0050431 arrhythmogenic right ventricular cardiomyopathy HGNC:3036 Homo sapiens (human) 1824 DSC2
  • MGI:6194238
  • PMID:24086444
  • PMID:25497880
DOID:0080042 autosomal recessive spinocerebellar ataxia 18 MGI:95813 Mus musculus (house mouse) 14804 Grid2
  • MGI:6194238
  • PMID:24078737
DOID:0080547 metabolic dysfunction-associated steatohepatitis RGD:619935 Rattus norvegicus (Norway rat) 294853 Krt18
  • MGI:6194238
  • PMID:24071521
DOID:0110481 autosomal recessive nonsyndromic deafness 23 MGI:1891428 Mus musculus (house mouse) 11994 Pcdh15
  • MGI:6194238
  • PMID:24044941
DOID:10283 prostate cancer MGI:1928480 Mus musculus (house mouse) 56318 Acp3
  • MGI:6194238
  • PMID:24039861
DOID:8947 diabetic retinopathy RGD:1598328 Rattus norvegicus (Norway rat) 310738 Ngf
  • MGI:6194238
  • PMID:24030532
DOID:0110334 osteogenesis imperfecta type 1 MGI:88467 Mus musculus (house mouse) 12842 Col1a1
  • MGI:6194238
  • PMID:2402497
DOID:9352 type 2 diabetes mellitus HGNC:23145 Homo sapiens (human) 389692 MAFA
  • MGI:6194238
  • PMID:24013263
DOID:1697 ichthyosis HGNC:6973 Homo sapiens (human) 4193 MDM2
  • MGI:6194238
  • PMID:24005053
DOID:11723 Duchenne muscular dystrophy HGNC:2928 Homo sapiens (human) 1756 DMD
  • MGI:6194238
  • PMID:23975932
  • PMID:24010700
  • PMID:3055295
  • RGD:7240710
DOID:0060649 congenital hereditary endothelial dystrophy of cornea MGI:2138987 Mus musculus (house mouse) 269356 Slc4a11
  • MGI:6194238
  • PMID:23942972
DOID:0060230 basal ganglia calcification MGI:97851 Mus musculus (house mouse) 20516 Slc20a2
  • MGI:6194238
  • PMID:23934451
DOID:11054 urinary bladder cancer MGI:88276 Mus musculus (house mouse) 12387 Ctnnb1
  • MGI:6194238
  • PMID:23928991
DOID:12236 primary biliary cholangitis HGNC:5971 Homo sapiens (human) 3594 IL12RB1
  • MGI:6194238
  • PMID:23910013
DOID:9970 obesity HGNC:4324 Homo sapiens (human) 2740 GLP1R
  • MGI:6194238
  • PMID:23900445
DOID:9970 obesity HGNC:11364 Homo sapiens (human) 6774 STAT3
  • MGI:6194238
  • PMID:23900445

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Last updated: December 9, 2024