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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 1201 - 1225 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID ▲ Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:417 autoimmune disease HGNC:270 Homo sapiens (human) 142 PARP1
  • PMID:16026592
DOID:10652 Alzheimer's disease HGNC:270 Homo sapiens (human) 142 PARP1
  • PMID:17290104
  • PMID:20486200
DOID:9352 type 2 diabetes mellitus HGNC:270 Homo sapiens (human) 142 PARP1
  • MGI:6194238
  • PMID:15895395
DOID:5199 ureteral obstruction HGNC:270 Homo sapiens (human) 142 PARP1
  • MGI:6194238
DOID:8677 perinatal necrotizing enterocolitis HGNC:270 Homo sapiens (human) 142 PARP1
  • MGI:6194238
  • PMID:21399558
DOID:10534 stomach cancer HGNC:270 Homo sapiens (human) 142 PARP1
  • PMID:29408335
  • PMID:32106377
DOID:0050156 idiopathic pulmonary fibrosis HGNC:270 Homo sapiens (human) 142 PARP1
  • PMID:23260200
DOID:5082 liver cirrhosis HGNC:270 Homo sapiens (human) 142 PARP1
  • PMID:25755481
DOID:10952 nephritis HGNC:270 Homo sapiens (human) 142 PARP1
  • PMID:16461442
DOID:9470 bacterial meningitis HGNC:270 Homo sapiens (human) 142 PARP1
  • PMID:21651918
DOID:127 leiomyoma HGNC:270 Homo sapiens (human) 142 PARP1
  • MGI:6194238
DOID:3525 middle cerebral artery infarction HGNC:270 Homo sapiens (human) 142 PARP1
  • MGI:6194238
DOID:5154 borna disease HGNC:270 Homo sapiens (human) 142 PARP1
  • MGI:6194238
DOID:2841 asthma HGNC:270 Homo sapiens (human) 142 PARP1
  • PMID:26205779
DOID:5844 myocardial infarction HGNC:2422 Homo sapiens (human) 1431 CS
  • MGI:6194238
DOID:12930 dilated cardiomyopathy HGNC:2422 Homo sapiens (human) 1431 CS
  • PMID:10354207
  • PMID:8252591
DOID:0050852 limb ischemia HGNC:2422 Homo sapiens (human) 1431 CS
  • MGI:6194238
DOID:11984 hypertrophic cardiomyopathy HGNC:2422 Homo sapiens (human) 1431 CS
  • PMID:10354207
DOID:7998 hyperthyroidism HGNC:2422 Homo sapiens (human) 1431 CS
  • MGI:6194238
DOID:1459 hypothyroidism HGNC:2422 Homo sapiens (human) 1431 CS
  • MGI:6194238
DOID:8466 retinal degeneration HGNC:2422 Homo sapiens (human) 1431 CS
  • MGI:6194238
DOID:3312 bipolar disorder HGNC:2422 Homo sapiens (human) 1431 CS
  • MGI:6194238
DOID:6000 congestive heart failure HGNC:2422 Homo sapiens (human) 1431 CS
  • MGI:6194238
DOID:219 colon cancer HGNC:6876 Homo sapiens (human) 1432 MAPK14
  • PMID:23027623
  • PMID:23859041
DOID:3717 gastric adenocarcinoma HGNC:6876 Homo sapiens (human) 1432 MAPK14
  • PMID:32243890

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Supported by JST NBDC Grant Number JPMJND2204

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Last updated: August 19, 2024