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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 61451 - 61475 of 71927 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol ▼ FlyGlycoDB Evidence Code Names References
DOID:0050742 nicotine dependence HGNC:2345 Homo sapiens (human) 1385 CREB1
  • PMID:20047710
DOID:9973 substance dependence HGNC:2345 Homo sapiens (human) 1385 CREB1
  • MGI:6194238
DOID:11206 opioid abuse HGNC:2345 Homo sapiens (human) 1385 CREB1
  • MGI:6194238
DOID:12858 Huntington's disease HGNC:2345 Homo sapiens (human) 1385 CREB1
  • MGI:6194238
DOID:3525 middle cerebral artery infarction HGNC:2345 Homo sapiens (human) 1385 CREB1
  • MGI:6194238
DOID:9975 cocaine dependence HGNC:2345 Homo sapiens (human) 1385 CREB1
  • MGI:6194238
  • PMID:19001277
DOID:10933 obsessive-compulsive disorder HGNC:2345 Homo sapiens (human) 1385 CREB1
  • MGI:6194238
DOID:9976 heroin dependence HGNC:2345 Homo sapiens (human) 1385 CREB1
  • MGI:6194238
  • PMID:24704376
DOID:10763 hypertension HGNC:2345 Homo sapiens (human) 1385 CREB1
  • MGI:6194238
DOID:10584 retinitis pigmentosa HGNC:18688 Homo sapiens (human) 286204 CRB2
  • MGI:6194238
DOID:0111134 focal segmental glomerulosclerosis 9 HGNC:18688 Homo sapiens (human) 286204 CRB2
  • RGD:7240710
DOID:0111625 ventriculomegaly - cystic kidney disease HGNC:18688 Homo sapiens (human) 286204 CRB2
  • RGD:7240710
DOID:10584 retinitis pigmentosa HGNC:2343 Homo sapiens (human) 23418 CRB1
  • MGI:6194238
  • PMID:10508521
  • PMID:20956273
DOID:14791 Leber congenital amaurosis HGNC:2343 Homo sapiens (human) 23418 CRB1
  • MGI:6194238
  • PMID:20956273
  • PMID:24715753
DOID:0110079 Leber congenital amaurosis 8 HGNC:2343 Homo sapiens (human) 23418 CRB1
  • MGI:6194238
  • RGD:7240710
DOID:0111541 pigmented paravenous chorioretinal atrophy HGNC:2343 Homo sapiens (human) 23418 CRB1
  • PMID:15623792
  • RGD:7240710
DOID:0110358 retinitis pigmentosa 12 HGNC:2343 Homo sapiens (human) 23418 CRB1
  • MGI:6194238
  • RGD:7240710
DOID:0050572 cone-rod dystrophy HGNC:2343 Homo sapiens (human) 23418 CRB1
  • PMID:23767994
DOID:0110734 neurodegeneration with brain iron accumulation HGNC:2342 Homo sapiens (human) 1384 CRAT
  • RGD:7240710
DOID:0081150 common variable immunodeficiency 7 HGNC:2336 Homo sapiens (human) 1380 CR2
  • RGD:7240710
DOID:526 human immunodeficiency virus infectious disease HGNC:2336 Homo sapiens (human) 1380 CR2
  • PMID:8442917
DOID:9261 nasopharynx carcinoma HGNC:2336 Homo sapiens (human) 1380 CR2
  • PMID:23612877
DOID:9074 systemic lupus erythematosus HGNC:2336 Homo sapiens (human) 1380 CR2
  • RGD:7240710
DOID:12365 malaria HGNC:2334 Homo sapiens (human) 1378 CR1
  • RGD:7240710
DOID:3146 lipid metabolism disorder FB:FBgn0035383 Drosophila melanogaster (fruit fly) 38355 CPT2
  • MGI:6194238

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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