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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 8576 - 8600 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID ▼ Species Gene ID Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:14115 toxic shock syndrome HGNC:3353 Homo sapiens (human) 2026 ENO2
  • MGI:6194238
DOID:11054 urinary bladder cancer HGNC:3353 Homo sapiens (human) 2026 ENO2
  • PMID:17951193
DOID:10763 hypertension HGNC:3353 Homo sapiens (human) 2026 ENO2
  • PMID:21130083
DOID:3459 breast carcinoma HGNC:3353 Homo sapiens (human) 2026 ENO2
  • PMID:16608642
DOID:1800 neuroendocrine carcinoma HGNC:3353 Homo sapiens (human) 2026 ENO2
  • PMID:15010880
DOID:11832 visual epilepsy HGNC:3353 Homo sapiens (human) 2026 ENO2
  • MGI:6194238
DOID:936 brain disease HGNC:3353 Homo sapiens (human) 2026 ENO2
  • PMID:20847541
DOID:12783 migraine without aura HGNC:3353 Homo sapiens (human) 2026 ENO2
  • PMID:21293918
DOID:10283 prostate cancer HGNC:3353 Homo sapiens (human) 2026 ENO2
  • PMID:15239127
DOID:10652 Alzheimer's disease HGNC:3350 Homo sapiens (human) 2023 ENO1
  • PMID:17387692
DOID:10763 hypertension HGNC:3350 Homo sapiens (human) 2023 ENO1
  • MGI:6194238
DOID:0110657 congenital myasthenic syndrome 8 HGNC:329 Homo sapiens (human) 375790 AGRN
  • MGI:6194238
  • RGD:7240710
DOID:0110853 rhizomelic chondrodysplasia punctata type 3 HGNC:327 Homo sapiens (human) 8540 AGPS
  • MGI:6194238
  • RGD:7240710
DOID:2580 rhizomelic chondrodysplasia punctata HGNC:327 Homo sapiens (human) 8540 AGPS
  • PMID:9553082
DOID:811 lipodystrophy HGNC:325 Homo sapiens (human) 10555 AGPAT2
  • PMID:11967537
DOID:0111135 congenital generalized lipodystrophy type 1 HGNC:325 Homo sapiens (human) 10555 AGPAT2
  • MGI:6194238
  • RGD:7240710
DOID:0080759 Fanconi renotubular syndrome 3 HGNC:3247 Homo sapiens (human) 1962 EHHADH
  • RGD:7240710
DOID:0080567 congenital disorder of glycosylation Ip HGNC:32456 Homo sapiens (human) 440138 ALG11
  • RGD:7240710
DOID:0060668 anencephaly HGNC:3225 Homo sapiens (human) 1946 EFNA5
  • MGI:6194238
DOID:2748 glycogen storage disease III HGNC:321 Homo sapiens (human) 178 AGL
  • MGI:6194238
  • PMID:16705713
  • RGD:7240710
DOID:4676 uremia HGNC:321 Homo sapiens (human) 178 AGL
  • MGI:6194238
DOID:8398 osteoarthritis HGNC:319 Homo sapiens (human) 176 ACAN
  • MGI:6194238
DOID:2377 multiple sclerosis HGNC:319 Homo sapiens (human) 176 ACAN
  • PMID:11764092
DOID:6000 congestive heart failure HGNC:319 Homo sapiens (human) 176 ACAN
  • MGI:6194238
DOID:1824 status epilepticus HGNC:319 Homo sapiens (human) 176 ACAN
  • MGI:6194238

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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