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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 8176 - 8200 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID ▼ Species Gene ID Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:0060363 glycerol kinase deficiency HGNC:4291 Homo sapiens (human) 2712 GK2
  • MGI:6194238
DOID:11054 urinary bladder cancer HGNC:429 Homo sapiens (human) 239 ALOX12
  • PMID:14532840
DOID:9970 obesity HGNC:429 Homo sapiens (human) 239 ALOX12
  • MGI:6194238
DOID:6000 congestive heart failure HGNC:429 Homo sapiens (human) 239 ALOX12
  • MGI:6194238
DOID:8893 psoriasis HGNC:429 Homo sapiens (human) 239 ALOX12
  • PMID:8304420
DOID:4450 renal cell carcinoma HGNC:429 Homo sapiens (human) 239 ALOX12
  • PMID:14654968
DOID:1612 breast cancer HGNC:429 Homo sapiens (human) 239 ALOX12
  • PMID:19282568
DOID:9352 type 2 diabetes mellitus HGNC:429 Homo sapiens (human) 239 ALOX12
  • PMID:9500559
DOID:10283 prostate cancer HGNC:429 Homo sapiens (human) 239 ALOX12
  • PMID:7624992
DOID:10763 hypertension HGNC:429 Homo sapiens (human) 239 ALOX12
  • MGI:6194238
DOID:8778 Crohn's disease HGNC:429 Homo sapiens (human) 239 ALOX12
  • PMID:7679252
DOID:8577 ulcerative colitis HGNC:429 Homo sapiens (human) 239 ALOX12
  • PMID:7679252
DOID:0060363 glycerol kinase deficiency HGNC:4289 Homo sapiens (human) 2710 GK
  • MGI:6194238
  • PMID:9719371
  • RGD:7240710
DOID:13810 familial hypercholesterolemia HGNC:4289 Homo sapiens (human) 2710 GK
  • MGI:6194238
DOID:684 hepatocellular carcinoma HGNC:4250 Homo sapiens (human) 2678 GGT1
  • PMID:10572675
  • PMID:11940314
  • PMID:27793641
DOID:13608 biliary atresia HGNC:4250 Homo sapiens (human) 2678 GGT1
  • PMID:29056230
DOID:0111257 gamma-glutamyl transpeptidase deficiency HGNC:4250 Homo sapiens (human) 2678 GGT1
  • RGD:7240710
DOID:9743 diabetic neuropathy HGNC:4250 Homo sapiens (human) 2678 GGT1
  • PMID:11311965
DOID:5082 liver cirrhosis HGNC:4250 Homo sapiens (human) 2678 GGT1
  • PMID:15997630
  • PMID:25254524
  • PMID:27793641
DOID:9352 type 2 diabetes mellitus HGNC:4250 Homo sapiens (human) 2678 GGT1
  • PMID:19936701
DOID:8947 diabetic retinopathy HGNC:4250 Homo sapiens (human) 2678 GGT1
  • PMID:11311965
DOID:5022 aflatoxins-related hepatocellular carcinoma HGNC:4250 Homo sapiens (human) 2678 GGT1
  • MGI:6194238
DOID:0050741 alcohol dependence HGNC:4250 Homo sapiens (human) 2678 GGT1
  • MGI:6194238
DOID:9351 diabetes mellitus HGNC:4250 Homo sapiens (human) 2678 GGT1
  • PMID:17888134
DOID:0080546 non-alcoholic fatty liver HGNC:4250 Homo sapiens (human) 2678 GGT1
  • PMID:23730648

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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