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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 11876 - 11900 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB Evidence Code Names ▲ References
DOID:11476 osteoporosis HGNC:2593 Homo sapiens (human) 1586 CYP17A1
  • PMID:17002564
DOID:0050453 lissencephaly HGNC:9202 Homo sapiens (human) 10585 POMT1
  • PMID:17559086
DOID:1059 intellectual disability HGNC:1938 Homo sapiens (human) 1120 CHKB
  • PMID:21665002
DOID:10159 osteonecrosis HGNC:1516 Homo sapiens (human) 847 CAT
  • PMID:18353692
DOID:14067 Plasmodium falciparum malaria HGNC:2621 Homo sapiens (human) 1557 CYP2C19
  • PMID:10471063
DOID:2841 asthma HGNC:15634 Homo sapiens (human) 81793 TLR10
  • PMID:18547625
DOID:3393 coronary artery disease HGNC:94 Homo sapiens (human) 39 ACAT2
  • PMID:16195894
DOID:10652 Alzheimer's disease HGNC:9232 Homo sapiens (human) 5465 PPARA
  • PMID:12938026
  • PMID:17850927
DOID:399 tuberculosis HGNC:2615 Homo sapiens (human) 1555 CYP2B6
  • PMID:28389387
  • PMID:30239753
DOID:9383 iridocyclitis HGNC:5344 Homo sapiens (human) 3383 ICAM1
  • PMID:20445114
DOID:5419 schizophrenia HGNC:6470 Homo sapiens (human) 3897 L1CAM
  • PMID:11425011
DOID:1588 thrombocytopenia HGNC:6922 Homo sapiens (human) 4153 MBL2
  • PMID:18361938
DOID:3146 lipid metabolism disorder HGNC:2330 Homo sapiens (human) 1376 CPT2
  • PMID:1528846
DOID:1612 breast cancer HGNC:2707 Homo sapiens (human) 1636 ACE
  • PMID:23828384
DOID:3393 coronary artery disease HGNC:11998 Homo sapiens (human) 7157 TP53
  • PMID:29482350
DOID:3649 pyruvate decarboxylase deficiency HGNC:21350 Homo sapiens (human) 8050 PDHX
  • RGD:7240710
DOID:6364 migraine HGNC:11892 Homo sapiens (human) 7124 TNF
  • RGD:7240710
DOID:0060448 Fleck corneal dystrophy HGNC:23785 Homo sapiens (human) 200576 PIKFYVE
  • RGD:7240710
DOID:2349 arteriosclerosis HGNC:435 Homo sapiens (human) 240 ALOX5
  • PMID:14702425
DOID:13544 low tension glaucoma HGNC:11998 Homo sapiens (human) 7157 TP53
  • PMID:20357201
DOID:1825 childhood absence epilepsy HGNC:11005 Homo sapiens (human) 6513 SLC2A1
  • PMID:26537434
DOID:10892 hypospadias HGNC:11285 Homo sapiens (human) 6716 SRD5A2
  • PMID:10514539
DOID:9352 type 2 diabetes mellitus HGNC:404 Homo sapiens (human) 217 ALDH2
  • PMID:15563966
DOID:5844 myocardial infarction HGNC:6623 Homo sapiens (human) 9388 LIPG
  • PMID:17526978
DOID:12849 autistic disorder HGNC:8978 Homo sapiens (human) 5294 PIK3CG
  • PMID:14627686

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Supported by JST NBDC Grant Number JPMJND2204

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Last updated: August 19, 2024