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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 October 9, 2024
Displaying entries 70701 - 70725 of 71927 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol ▼ FlyGlycoDB Evidence Code Names References
DOID:6000 congestive heart failure HGNC:336 Homo sapiens (human) 185 AGTR1
  • MGI:6194238
DOID:1073 renal hypertension HGNC:336 Homo sapiens (human) 185 AGTR1
  • MGI:6194238
DOID:10763 hypertension HGNC:336 Homo sapiens (human) 185 AGTR1
  • MGI:6194238
  • PMID:16519598
  • PMID:9456365
DOID:4780 anti-basement membrane glomerulonephritis HGNC:336 Homo sapiens (human) 185 AGTR1
  • MGI:6194238
DOID:5844 myocardial infarction HGNC:336 Homo sapiens (human) 185 AGTR1
  • MGI:6194238
  • PMID:16061119
  • PMID:9857918
DOID:11984 hypertrophic cardiomyopathy HGNC:333 Homo sapiens (human) 183 AGT
  • PMID:9023164
  • PMID:9270088
DOID:11446 sciatic neuropathy HGNC:333 Homo sapiens (human) 183 AGT
  • MGI:6194238
DOID:5082 liver cirrhosis HGNC:333 Homo sapiens (human) 183 AGT
  • MGI:6194238
DOID:418 systemic scleroderma HGNC:333 Homo sapiens (human) 183 AGT
  • PMID:17360781
DOID:6713 cerebrovascular disease HGNC:333 Homo sapiens (human) 183 AGT
  • PMID:17220293
DOID:1580 diffuse scleroderma HGNC:333 Homo sapiens (human) 183 AGT
  • PMID:14730619
DOID:1612 breast cancer HGNC:333 Homo sapiens (human) 183 AGT
  • PMID:16823505
  • PMID:23374911
  • PMID:23828384
DOID:1875 impotence HGNC:333 Homo sapiens (human) 183 AGT
  • MGI:6194238
DOID:8923 skin melanoma HGNC:333 Homo sapiens (human) 183 AGT
  • PMID:19394758
DOID:2921 glomerulonephritis HGNC:333 Homo sapiens (human) 183 AGT
  • MGI:6194238
DOID:3328 temporal lobe epilepsy HGNC:333 Homo sapiens (human) 183 AGT
  • MGI:6194238
DOID:12930 dilated cardiomyopathy HGNC:333 Homo sapiens (human) 183 AGT
  • MGI:6194238
  • PMID:9270088
DOID:11123 Henoch-Schoenlein purpura HGNC:333 Homo sapiens (human) 183 AGT
  • PMID:16521052
  • PMID:20702504
DOID:4780 anti-basement membrane glomerulonephritis HGNC:333 Homo sapiens (human) 183 AGT
  • MGI:6194238
DOID:8805 intermediate coronary syndrome HGNC:333 Homo sapiens (human) 183 AGT
  • PMID:11451295
DOID:3407 carotid artery disease HGNC:333 Homo sapiens (human) 183 AGT
  • PMID:17220293
DOID:8947 diabetic retinopathy HGNC:333 Homo sapiens (human) 183 AGT
  • MGI:6194238
  • PMID:10862638
DOID:0060224 atrial fibrillation HGNC:333 Homo sapiens (human) 183 AGT
  • PMID:18239384
DOID:11396 pulmonary edema HGNC:333 Homo sapiens (human) 183 AGT
  • PMID:21393362
DOID:224 transient cerebral ischemia HGNC:333 Homo sapiens (human) 183 AGT
  • MGI:6194238

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GlyCosmos is a member of the GlySpace Alliance together with GlyGen and Glycomics@ExPASy.

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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: December 9, 2024