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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 71301 - 71325 of 71927 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID ▼ Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:1612 breast cancer HGNC:336 Homo sapiens (human) 185 AGTR1
  • PMID:23828384
DOID:1312 focal segmental glomerulosclerosis HGNC:336 Homo sapiens (human) 185 AGTR1
  • MGI:6194238
DOID:2986 IgA glomerulonephritis HGNC:336 Homo sapiens (human) 185 AGTR1
  • PMID:15930094
DOID:9620 vesicoureteral reflux HGNC:336 Homo sapiens (human) 185 AGTR1
  • PMID:11819209
DOID:0050851 glomerulosclerosis 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:2018 hyperinsulinism HGNC:336 Homo sapiens (human) 185 AGTR1
  • MGI:6194238
DOID:6713 cerebrovascular disease HGNC:336 Homo sapiens (human) 185 AGTR1
  • PMID:16109907
DOID:11335 sarcoidosis HGNC:336 Homo sapiens (human) 185 AGTR1
  • PMID:20560294
  • PMID:21319597
DOID:8805 intermediate coronary syndrome HGNC:336 Homo sapiens (human) 185 AGTR1
  • PMID:11451295
DOID:3407 carotid artery disease HGNC:336 Homo sapiens (human) 185 AGTR1
  • PMID:16519598
DOID:10952 nephritis HGNC:336 Homo sapiens (human) 185 AGTR1
  • MGI:6194238
DOID:1591 renovascular hypertension HGNC:336 Homo sapiens (human) 185 AGTR1
  • MGI:6194238
DOID:576 proteinuria HGNC:336 Homo sapiens (human) 185 AGTR1
  • MGI:6194238
DOID:784 chronic kidney disease HGNC:336 Homo sapiens (human) 185 AGTR1
  • MGI:6194238
  • PMID:12832734
DOID:5844 myocardial infarction HGNC:336 Homo sapiens (human) 185 AGTR1
  • MGI:6194238
  • PMID:16061119
  • PMID:9857918
DOID:3891 placental insufficiency HGNC:336 Homo sapiens (human) 185 AGTR1
  • MGI:6194238
DOID:3393 coronary artery disease HGNC:336 Homo sapiens (human) 185 AGTR1
  • PMID:12975417
DOID:12858 Huntington's disease HGNC:336 Homo sapiens (human) 185 AGTR1
  • PMID:8666063
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:10825 essential hypertension HGNC:336 Homo sapiens (human) 185 AGTR1
  • PMID:18604484
  • RGD:7240710
DOID:0060224 atrial fibrillation HGNC:336 Homo sapiens (human) 185 AGTR1
  • PMID:20080265
DOID:2841 asthma HGNC:336 Homo sapiens (human) 185 AGTR1
  • MGI:6194238
DOID:4450 renal cell carcinoma HGNC:336 Homo sapiens (human) 185 AGTR1
  • PMID:21102591

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Supported by JST NBDC Grant Number JPMJND2204

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