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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 3801 - 3825 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID Species ▲ Gene ID Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:10128 venous insufficiency HGNC:5344 Homo sapiens (human) 3383 ICAM1
  • PMID:25495610
DOID:1936 atherosclerosis HGNC:26876 Homo sapiens (human) 165631 PARP15
  • PMID:33381146
DOID:874 bacterial pneumonia HGNC:10798 Homo sapiens (human) 653509 SFTPA1
  • MGI:6194238
DOID:3908 lung non-small cell carcinoma HGNC:5383 Homo sapiens (human) 3418 IDH2
  • PMID:25576295
DOID:1574 alcohol use disorder HGNC:5466 Homo sapiens (human) 3481 IGF2
  • PMID:30277635
DOID:2671 transitional cell carcinoma HGNC:8125 Homo sapiens (human) 4968 OGG1
  • PMID:22110223
DOID:1849 cannabis dependence HGNC:2228 Homo sapiens (human) 1312 COMT
  • PMID:24902721
DOID:3083 chronic obstructive pulmonary disease HGNC:2596 Homo sapiens (human) 1544 CYP1A2
  • PMID:20080081
DOID:5844 myocardial infarction HGNC:9056 Homo sapiens (human) 5331 PLCB3
  • MGI:6194238
DOID:4362 cervical cancer HGNC:2665 Homo sapiens (human) 1604 CD55
  • PMID:9358772
DOID:422 congenital structural myopathy HGNC:7448 Homo sapiens (human) 4534 MTM1
  • PMID:8640223
DOID:1432 blindness HGNC:24768 Homo sapiens (human) 375775 PNPLA7
  • MGI:6194238
DOID:0050571 congenital disorder of glycosylation type II HGNC:4124 Homo sapiens (human) 2590 GALNT2
  • RGD:7240710
DOID:1214 tympanosclerosis HGNC:1516 Homo sapiens (human) 847 CAT
  • PMID:14710000
DOID:5199 ureteral obstruction HGNC:391 Homo sapiens (human) 207 AKT1
  • MGI:6194238
DOID:8466 retinal degeneration HGNC:9059 Homo sapiens (human) 5332 PLCB4
  • MGI:6194238
DOID:9470 bacterial meningitis HGNC:1932 Homo sapiens (human) 1116 CHI3L1
  • PMID:11986266
DOID:0070330 multiple mitochondrial dysfunctions syndrome HGNC:4208 Homo sapiens (human) 2653 GCSH
  • RGD:7240710
DOID:10763 hypertension HGNC:4923 Homo sapiens (human) 3099 HK2
  • MGI:6194238
DOID:2394 ovarian cancer HGNC:1932 Homo sapiens (human) 1116 CHI3L1
  • PMID:12883737
DOID:11446 sciatic neuropathy HGNC:1516 Homo sapiens (human) 847 CAT
  • MGI:6194238
DOID:162 cancer HGNC:392 Homo sapiens (human) 208 AKT2
  • MGI:6194238
DOID:0060892 late onset Parkinson's disease HGNC:251 Homo sapiens (human) 126 ADH1C
  • RGD:7240710
DOID:2349 arteriosclerosis HGNC:6554 Homo sapiens (human) 3953 LEPR
  • PMID:11460888
DOID:1070 primary open angle glaucoma HGNC:6922 Homo sapiens (human) 4153 MBL2
  • PMID:22335808

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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