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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 67976 - 68000 of 71927 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB Evidence Code Names ▲ References
DOID:14695 galactokinase deficiency HGNC:4118 Homo sapiens (human) 2584 GALK1
  • RGD:7240710
DOID:8778 Crohn's disease HGNC:19100 Homo sapiens (human) 149233 IL23R
  • PMID:17068223
DOID:3121 gallbladder cancer HGNC:12828 Homo sapiens (human) 7515 XRCC1
  • PMID:19266243
DOID:3312 bipolar disorder HGNC:6922 Homo sapiens (human) 4153 MBL2
  • PMID:24856568
DOID:11555 Fuchs' endothelial dystrophy HGNC:11642 Homo sapiens (human) 6935 ZEB1
  • RGD:7240710
DOID:0050741 alcohol dependence HGNC:1963 Homo sapiens (human) 1142 CHRNB3
  • PMID:24057674
DOID:612 primary immunodeficiency disease HGNC:10937 Homo sapiens (human) 6573 SLC19A1
  • RGD:7240710
DOID:8577 ulcerative colitis HGNC:40 Homo sapiens (human) 5243 ABCB1
  • PMID:15505619
DOID:0080528 bronchiectasis 3 HGNC:10602 Homo sapiens (human) 6340 SCNN1G
  • RGD:7240710
DOID:2256 osteochondrodysplasia HGNC:2217 Homo sapiens (human) 1297 COL9A1
  • PMID:11565064
DOID:10159 osteonecrosis HGNC:9051 Homo sapiens (human) 5327 PLAT
  • PMID:24025446
DOID:0110014 age related macular degeneration 1 HGNC:19194 Homo sapiens (human) 83872 HMCN1
  • RGD:7240710
DOID:1205 allergic disease HGNC:333 Homo sapiens (human) 183 AGT
  • PMID:10200023
DOID:0080501 GM1 gangliosidosis type 2 HGNC:4298 Homo sapiens (human) 2720 GLB1
  • RGD:7240710
DOID:9952 acute lymphoblastic leukemia HGNC:6119 Homo sapiens (human) 3662 IRF4
  • PMID:19897031
DOID:0112115 combined oxidative phosphorylation deficiency 46 HGNC:14509 Homo sapiens (human) 51649 MRPS23
  • RGD:7240710
DOID:0111052 Scott syndrome HGNC:25240 Homo sapiens (human) 196527 ANO6
  • RGD:7240710
DOID:526 human immunodeficiency virus infectious disease HGNC:2615 Homo sapiens (human) 1555 CYP2B6
  • PMID:18281305
  • PMID:21862974
DOID:0050978 spinocerebellar ataxia type 29 HGNC:6180 Homo sapiens (human) 3708 ITPR1
  • RGD:7240710
DOID:1324 lung cancer HGNC:1957 Homo sapiens (human) 1136 CHRNA3
  • PMID:19491260
  • PMID:22441734
  • PMID:23023782
  • PMID:23056235
  • PMID:29416783
  • PMID:29993116
  • RGD:7240710
DOID:2738 pseudoxanthoma elasticum HGNC:1516 Homo sapiens (human) 847 CAT
  • PMID:17693525
DOID:5353 colonic disease HGNC:4263 Homo sapiens (human) 2690 GHR
  • PMID:19864451
DOID:3393 coronary artery disease HGNC:610 Homo sapiens (human) 345 APOC3
  • PMID:14709372
  • PMID:15059615
DOID:0050127 sinusitis HGNC:1884 Homo sapiens (human) 1080 CFTR
  • PMID:11773581
DOID:3393 coronary artery disease HGNC:12744 Homo sapiens (human) 51085 MLXIPL
  • PMID:19571538
  • PMID:21726544
  • PMID:25179879

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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