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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 4776 - 4800 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID Species ▲ Gene ID Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:2998 testicular cancer HGNC:11998 Homo sapiens (human) 7157 TP53
  • MGI:6194238
DOID:10763 hypertension HGNC:9232 Homo sapiens (human) 5465 PPARA
  • MGI:6194238
DOID:13580 cholestasis HGNC:1516 Homo sapiens (human) 847 CAT
  • MGI:6194238
DOID:0050558 Ullrich congenital muscular dystrophy HGNC:2211 Homo sapiens (human) 1291 COL6A1
  • MGI:6194238
  • RGD:7240710
DOID:13636 Fanconi anemia HGNC:11892 Homo sapiens (human) 7124 TNF
  • PMID:24021704
  • PMID:8438880
DOID:3458 breast adenocarcinoma HGNC:1516 Homo sapiens (human) 847 CAT
  • PMID:25050522
DOID:0070382 developmental and epileptic encephalopathy 95 HGNC:14937 Homo sapiens (human) 94005 PIGS
  • RGD:7240710
DOID:1612 breast cancer HGNC:2873 Homo sapiens (human) 1727 CYB5R3
  • PMID:25225034
DOID:5154 borna disease HGNC:1681 Homo sapiens (human) 960 CD44
  • MGI:6194238
DOID:1324 lung cancer HGNC:9605 Homo sapiens (human) 5743 PTGS2
  • MGI:6194238
DOID:10763 hypertension HGNC:4617 Homo sapiens (human) 2932 GSK3B
  • MGI:6194238
DOID:12361 Graves' disease HGNC:2595 Homo sapiens (human) 1543 CYP1A1
  • PMID:19903800
DOID:9563 bronchiectasis HGNC:11892 Homo sapiens (human) 7124 TNF
  • PMID:18221721
DOID:3659 sialuria HGNC:10933 Homo sapiens (human) 26503 SLC17A5
  • MGI:6194238
  • PMID:10581036
  • RGD:7240710
DOID:9778 irritable bowel syndrome HGNC:4606 Homo sapiens (human) 2923 PDIA3
  • MGI:6194238
DOID:0111103 maturity-onset diabetes of the young type 4 HGNC:6107 Homo sapiens (human) 3651 PDX1
  • MGI:6194238
  • RGD:7240710
DOID:0081267 graft-versus-host disease HGNC:11998 Homo sapiens (human) 7157 TP53
  • PMID:16393253
DOID:0111225 centronuclear myopathy X-linked HGNC:7448 Homo sapiens (human) 4534 MTM1
  • MGI:6194238
DOID:0080855 Parkinsonism HGNC:2228 Homo sapiens (human) 1312 COMT
  • MGI:6194238
DOID:2237 hepatitis HGNC:79 Homo sapiens (human) 28 ABO
  • PMID:32379894
DOID:0110196 Charcot-Marie-Tooth disease type 4G HGNC:4922 Homo sapiens (human) 3098 HK1
  • RGD:7240710
DOID:4247 coronary restenosis HGNC:11892 Homo sapiens (human) 7124 TNF
  • PMID:16319143
DOID:10286 prostate carcinoma HGNC:1932 Homo sapiens (human) 1116 CHI3L1
  • PMID:16372331
DOID:0050700 cardiomyopathy HGNC:9202 Homo sapiens (human) 10585 POMT1
  • PMID:22549409
DOID:10534 stomach cancer HGNC:1455 Homo sapiens (human) 811 CALR
  • PMID:19050968
  • PMID:31725767

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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