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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 68326 - 68350 of 71927 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB Evidence Code Names ▼ References
DOID:1793 pancreatic cancer HGNC:5246 Homo sapiens (human) 3315 HSPB1
  • PMID:21833720
DOID:10286 prostate carcinoma HGNC:786 Homo sapiens (human) 468 ATF4
  • PMID:25680860
DOID:0081267 graft-versus-host disease HGNC:2505 Homo sapiens (human) 1493 CTLA4
  • PMID:7515723
DOID:12930 dilated cardiomyopathy HGNC:6180 Homo sapiens (human) 3708 ITPR1
  • PMID:8567977
DOID:0050214 Lambert-Eaton myasthenic syndrome HGNC:1389 Homo sapiens (human) 774 CACNA1B
  • PMID:16289869
DOID:3168 squamous cell neoplasm HGNC:30796 Homo sapiens (human) 11171 STRAP
  • PMID:16778189
DOID:684 hepatocellular carcinoma HGNC:6001 Homo sapiens (human) 3558 IL2
  • PMID:10933975
  • PMID:9449371
DOID:1936 atherosclerosis HGNC:12692 Homo sapiens (human) 7431 VIM
  • PMID:21362765
DOID:1793 pancreatic cancer HGNC:3387 Homo sapiens (human) 2042 EPHA3
  • PMID:14670182
DOID:13268 porphyria HGNC:3415 Homo sapiens (human) 2056 EPO
  • PMID:17435269
DOID:0111902 thrombophilia due to activated protein C resistance HGNC:9451 Homo sapiens (human) 5624 PROC
  • PMID:25196808
DOID:6432 pulmonary hypertension RGD:61927 Rattus norvegicus (Norway rat) 29583 Pecam1
  • PMID:22559233
DOID:13141 uveitis RGD:70992 Rattus norvegicus (Norway rat) 113893 Sncb
  • PMID:12496452
DOID:10286 prostate carcinoma HGNC:11255 Homo sapiens (human) 6696 SPP1
  • PMID:16331611
DOID:0081292 traumatic brain injury HGNC:620 Homo sapiens (human) 351 APP
  • PMID:29320530
DOID:11446 sciatic neuropathy RGD:620630 Rattus norvegicus (Norway rat) 85268 Hrh3
  • PMID:17350523
DOID:0080208 metabolic dysfunction-associated steatotic liver disease HGNC:11764 Homo sapiens (human) 7038 TG
  • PMID:30016121
DOID:12704 ataxia telangiectasia HGNC:6001 Homo sapiens (human) 3558 IL2
  • PMID:6432389
DOID:820 myocarditis RGD:3752 Rattus norvegicus (Norway rat) 25353 Spp1
  • PMID:16679731
DOID:12306 vitiligo HGNC:12442 Homo sapiens (human) 7299 TYR
  • PMID:22834951
  • PMID:8697641
DOID:0050731 vitamin B12 deficiency RGD:708418 Rattus norvegicus (Norway rat) 84349 Cd40lg
  • PMID:16716410
DOID:3492 mixed connective tissue disease HGNC:11157 Homo sapiens (human) 6631 SNRPC
  • PMID:10555891
DOID:8991 cervix uteri carcinoma in situ HGNC:1748 Homo sapiens (human) 999 CDH1
  • PMID:17894941
DOID:10283 prostate cancer HGNC:5960 Homo sapiens (human) 3551 IKBKB
  • PMID:26435478
DOID:1407 anterior uveitis HGNC:11850 Homo sapiens (human) 7099 TLR4
  • PMID:17389503

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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