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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 66351 - 66375 of 71927 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB Evidence Code Names ▲ References
DOID:8544 chronic fatigue syndrome HGNC:12338 Homo sapiens (human) 7225 TRPC6
  • PMID:27834303
DOID:13141 uveitis HGNC:4931 Homo sapiens (human) 3105 HLA-A
  • PMID:20868569
DOID:11162 respiratory failure HGNC:6922 Homo sapiens (human) 4153 MBL2
  • PMID:18582923
DOID:9256 colorectal cancer HGNC:6307 Homo sapiens (human) 3791 KDR
  • PMID:22182247
DOID:0112062 immunodeficiency 73c with defective neutrophil chemotaxis and hypogammaglobulinemia HGNC:9802 Homo sapiens (human) 5880 RAC2
  • RGD:7240710
DOID:1380 endometrial cancer HGNC:12530 Homo sapiens (human) 54658 UGT1A1
  • PMID:18349273
DOID:0080599 Coronavirus infectious disease HGNC:6922 Homo sapiens (human) 4153 MBL2
  • PMID:15838797
DOID:1682 congenital heart disease HGNC:9969 Homo sapiens (human) 5981 RFC1
  • PMID:24585533
DOID:11702 dysgammaglobulinemia HGNC:12572 Homo sapiens (human) 7374 UNG
  • PMID:12958596
DOID:0060717 autosomal recessive congenital ichthyosis 8 HGNC:23452 Homo sapiens (human) 643418 LIPN
  • RGD:7240710
DOID:4481 allergic rhinitis HGNC:5973 Homo sapiens (human) 3596 IL13
  • PMID:12928861
  • PMID:17091279
  • PMID:22852128
  • PMID:23996716
  • RGD:7240710
DOID:14330 Parkinson's disease HGNC:1569 Homo sapiens (human) 885 CCK
  • PMID:10668930
DOID:0081426 autosomal recessive distal hereditary motor neuronopathy 7 HGNC:30910 Homo sapiens (human) 64856 VWA1
  • RGD:7240710
DOID:2394 ovarian cancer HGNC:4886 Homo sapiens (human) 3077 HFE
  • PMID:16216474
DOID:9351 diabetes mellitus HGNC:2527 Homo sapiens (human) 1508 CTSB
  • PMID:18706099
DOID:0081147 common variable immunodeficiency 4 HGNC:17755 Homo sapiens (human) 115650 TNFRSF13C
  • RGD:7240710
DOID:2559 opiate dependence HGNC:40 Homo sapiens (human) 5243 ABCB1
  • PMID:17178268
  • PMID:24086514
  • PMID:24950410
  • PMID:27061230
DOID:0050645 arterial tortuosity syndrome HGNC:3219 Homo sapiens (human) 30008 EFEMP2
  • PMID:22943132
DOID:6543 acne HGNC:6015 Homo sapiens (human) 3566 IL4R
  • PMID:22705603
DOID:7148 rheumatoid arthritis HGNC:1142 Homo sapiens (human) 56244 BTNL2
  • PMID:23364395
DOID:1612 breast cancer HGNC:7325 Homo sapiens (human) 4436 MSH2
  • PMID:16252083
DOID:10941 intracranial aneurysm HGNC:2464 Homo sapiens (human) 1462 VCAN
  • PMID:16917090
DOID:4947 cholangiocarcinoma HGNC:8125 Homo sapiens (human) 4968 OGG1
  • PMID:11260864
  • PMID:11866974
DOID:4449 macular retinal edema HGNC:7876 Homo sapiens (human) 4846 NOS3
  • PMID:15333482
DOID:11054 urinary bladder cancer HGNC:6844 Homo sapiens (human) 6416 MAP2K4
  • PMID:15665277

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International Collaboration

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