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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 66176 - 66200 of 71927 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB Evidence Code Names ▲ References
DOID:1380 endometrial cancer HGNC:1748 Homo sapiens (human) 999 CDH1
  • RGD:7240710
DOID:1793 pancreatic cancer HGNC:7218 Homo sapiens (human) 4353 MPO
  • PMID:18205184
DOID:9352 type 2 diabetes mellitus HGNC:1511 Homo sapiens (human) 842 CASP9
  • PMID:16038259
DOID:9253 gastrointestinal stromal tumor HGNC:18420 Homo sapiens (human) 29072 SETD2
  • PMID:26338826
DOID:9478 postpartum depression HGNC:12008 Homo sapiens (human) 7166 TPH1
  • PMID:15544576
DOID:12449 aplastic anemia HGNC:9360 Homo sapiens (human) 5551 PRF1
  • RGD:7240710
DOID:3454 brain infarction HGNC:20580 Homo sapiens (human) 120227 CYP2R1
  • PMID:36762557
DOID:1380 endometrial cancer HGNC:3229 Homo sapiens (human) 1950 EGF
  • PMID:19319135
DOID:3393 coronary artery disease HGNC:6677 Homo sapiens (human) 4023 LPL
  • PMID:8641022
DOID:811 lipodystrophy HGNC:325 Homo sapiens (human) 10555 AGPAT2
  • PMID:11967537
DOID:0050986 spinocerebellar ataxia type 40 HGNC:19967 Homo sapiens (human) 440193 CCDC88C
  • RGD:7240710
DOID:0111043 glycogen storage disease IXc HGNC:8931 Homo sapiens (human) 5261 PHKG2
  • RGD:7240710
DOID:1272 telangiectasis HGNC:7876 Homo sapiens (human) 4846 NOS3
  • PMID:18027873
DOID:0110994 Joubert syndrome 25 HGNC:24866 Homo sapiens (human) 9731 CEP104
  • RGD:7240710
DOID:627 severe combined immunodeficiency HGNC:12858 Homo sapiens (human) 7535 ZAP70
  • PMID:8124727
DOID:1574 alcohol use disorder HGNC:404 Homo sapiens (human) 217 ALDH2
  • PMID:10780266
DOID:627 severe combined immunodeficiency HGNC:1673 Homo sapiens (human) 915 CD3D
  • PMID:14602880
DOID:302 substance abuse HGNC:11050 Homo sapiens (human) 6532 SLC6A4
  • PMID:21140256
DOID:14067 Plasmodium falciparum malaria HGNC:2621 Homo sapiens (human) 1557 CYP2C19
  • PMID:10471063
DOID:0080502 GM1 gangliosidosis type 1 HGNC:4298 Homo sapiens (human) 2720 GLB1
  • RGD:7240710
DOID:12858 Huntington's disease HGNC:11741 Homo sapiens (human) 7019 TFAM
  • PMID:21595933
DOID:11984 hypertrophic cardiomyopathy HGNC:2707 Homo sapiens (human) 1636 ACE
  • PMID:9270088
DOID:0080939 hereditary angioedema type I HGNC:1228 Homo sapiens (human) 710 SERPING1
  • RGD:7240710
DOID:3969 thyroid gland papillary carcinoma HGNC:7989 Homo sapiens (human) 4893 NRAS
  • RGD:7240710
DOID:627 severe combined immunodeficiency HGNC:11566 Homo sapiens (human) 6892 TAPBP
  • PMID:12149238

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

Acknowledgements

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