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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 6701 - 6725 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID Species ▲ Gene ID Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:0060180 colitis HGNC:5344 Homo sapiens (human) 3383 ICAM1
  • MGI:6194238
DOID:890 mitochondrial encephalomyopathy HGNC:3148 Homo sapiens (human) 1890 TYMP
  • PMID:9924029
DOID:12236 primary biliary cholangitis HGNC:2707 Homo sapiens (human) 1636 ACE
  • MGI:6194238
DOID:0080208 metabolic dysfunction-associated steatotic liver disease HGNC:84 Homo sapiens (human) 31 ACACA
  • MGI:6194238
DOID:9970 obesity HGNC:392 Homo sapiens (human) 208 AKT2
  • MGI:6194238
  • PMID:12663464
DOID:11836 clubfoot HGNC:2595 Homo sapiens (human) 1543 CYP1A1
  • PMID:21254355
DOID:9352 type 2 diabetes mellitus HGNC:392 Homo sapiens (human) 208 AKT2
  • MGI:6194238
  • PMID:15166380
  • PMID:18204829
  • PMID:18972094
  • RGD:7240710
DOID:684 hepatocellular carcinoma HGNC:8976 Homo sapiens (human) 5291 PIK3CB
  • MGI:6194238
DOID:10763 hypertension HGNC:3402 Homo sapiens (human) 2053 EPHX2
  • MGI:6194238
  • PMID:20065888
DOID:0050827 rheumatic heart disease HGNC:1641 Homo sapiens (human) 30835 CD209
  • PMID:30261069
DOID:854 collagen disease HGNC:11850 Homo sapiens (human) 7099 TLR4
  • MGI:6194238
DOID:8893 psoriasis HGNC:11848 Homo sapiens (human) 7097 TLR2
  • PMID:23457721
DOID:0060180 colitis HGNC:9605 Homo sapiens (human) 5743 PTGS2
  • MGI:6194238
DOID:10763 hypertension HGNC:12524 Homo sapiens (human) 7357 UGCG
  • MGI:6194238
DOID:4621 holoprosencephaly HGNC:25712 Homo sapiens (human) 80055 PGAP1
  • MGI:6194238
DOID:0050814 temtamy preaxial brachydactyly syndrome HGNC:17198 Homo sapiens (human) 22856 CHSY1
  • RGD:7240710
DOID:2841 asthma HGNC:9040 Homo sapiens (human) 7941 PLA2G7
  • PMID:10733466
DOID:11054 urinary bladder cancer HGNC:1753 Homo sapiens (human) 1012 CDH13
  • PMID:18094410
DOID:9970 obesity HGNC:85 Homo sapiens (human) 32 ACACB
  • MGI:6194238
DOID:9970 obesity HGNC:18448 Homo sapiens (human) 79661 NEIL1
  • MGI:6194238
DOID:3905 lung carcinoma HGNC:2707 Homo sapiens (human) 1636 ACE
  • PMID:183595
DOID:874 bacterial pneumonia HGNC:2634 Homo sapiens (human) 1573 CYP2J2
  • MGI:6194238
DOID:9206 Barrett's esophagus HGNC:922 Homo sapiens (human) 135152 B3GAT2
  • PMID:26545406
DOID:11612 polycystic ovary syndrome HGNC:5217 Homo sapiens (human) 3283 HSD3B1
  • MGI:6194238
DOID:0050742 nicotine dependence HGNC:7656 Homo sapiens (human) 4684 NCAM1
  • PMID:17085484

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Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01


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