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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 3026 - 3050 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID Species ▲ Gene ID Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:5419 schizophrenia HGNC:9605 Homo sapiens (human) 5743 PTGS2
  • MGI:6194238
DOID:10652 Alzheimer's disease HGNC:10720 Homo sapiens (human) 6402 SELL
  • PMID:21484243
DOID:13564 aspergillosis HGNC:14558 Homo sapiens (human) 64581 CLEC7A
  • RGD:7240710
DOID:9119 acute myeloid leukemia HGNC:5383 Homo sapiens (human) 3418 IDH2
  • PMID:20368543
  • PMID:25324972
DOID:3312 bipolar disorder HGNC:2228 Homo sapiens (human) 1312 COMT
  • PMID:16984965
DOID:11400 pyelonephritis HGNC:2707 Homo sapiens (human) 1636 ACE
  • PMID:10504496
DOID:0070264 congenital disorder of glycosylation type IIl HGNC:18621 Homo sapiens (human) 57511 COG6
  • RGD:7240710
DOID:0060470 salt and pepper syndrome HGNC:10872 Homo sapiens (human) 8869 ST3GAL5
  • RGD:7240710
DOID:4159 skin cancer HGNC:545 Homo sapiens (human) 310 ANXA7
  • PMID:17708571
DOID:9352 type 2 diabetes mellitus HGNC:2622 Homo sapiens (human) 1558 CYP2C8
  • MGI:6194238
DOID:13276 Mycoplasma pneumoniae pneumonia HGNC:11892 Homo sapiens (human) 7124 TNF
  • PMID:20416219
DOID:5463 cochlear disease HGNC:11892 Homo sapiens (human) 7124 TNF
  • MGI:6194238
DOID:9970 obesity HGNC:936 Homo sapiens (human) 572 BAD
  • MGI:6194238
DOID:0080855 Parkinsonism HGNC:23 Homo sapiens (human) 18 ABAT
  • MGI:6194238
DOID:12858 Huntington's disease HGNC:4558 Homo sapiens (human) 257202 GPX6
  • PMID:18588971
DOID:0060189 ileitis HGNC:11848 Homo sapiens (human) 7097 TLR2
  • MGI:6194238
DOID:409 liver disease HGNC:404 Homo sapiens (human) 217 ALDH2
  • PMID:16408483
DOID:219 colon cancer HGNC:391 Homo sapiens (human) 207 AKT1
  • MGI:6194238
  • PMID:31932471
DOID:9352 type 2 diabetes mellitus HGNC:8971 Homo sapiens (human) 5286 PIK3C2A
  • PMID:21127054
DOID:2841 asthma HGNC:1628 Homo sapiens (human) 929 CD14
  • PMID:15741437
  • PMID:15940135
  • PMID:16387800
  • PMID:18312481
  • PMID:19096003
DOID:0060041 autism spectrum disorder HGNC:7681 Homo sapiens (human) 8509 NDST2
  • MGI:6194238
DOID:3310 atopic dermatitis HGNC:10721 Homo sapiens (human) 6403 SELP
  • PMID:12929084
DOID:10763 hypertension HGNC:2645 Homo sapiens (human) 8529 CYP4F2
  • MGI:6194238
DOID:9970 obesity HGNC:4922 Homo sapiens (human) 3098 HK1
  • MGI:6194238
  • PMID:131232
DOID:3312 bipolar disorder HGNC:6051 Homo sapiens (human) 3613 IMPA2
  • PMID:11673796
  • PMID:14699425
  • PMID:9322233

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Supported by JST NBDC Grant Number JPMJND2204

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


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Last updated: August 19, 2024