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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 63951 - 63975 of 71927 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB Evidence Code Names References ▲
DOID:0081294 neuronal intranuclear inclusion disease HGNC:17142 Homo sapiens (human) 10133 OPTN
  • PMID:22318854
DOID:12858 Huntington's disease HGNC:17142 Homo sapiens (human) 10133 OPTN
  • PMID:22318854
DOID:1184 nephrotic syndrome HGNC:11760 Homo sapiens (human) 7035 TFPI
  • PMID:22319062
DOID:0050745 diffuse large B-cell lymphoma HGNC:9346 Homo sapiens (human) 639 PRDM1
  • PMID:22321048
DOID:0060074 ductal carcinoma in situ HGNC:533 Homo sapiens (human) 301 ANXA1
  • PMID:22323911
DOID:3525 middle cerebral artery infarction HGNC:10848 Homo sapiens (human) 6469 SHH
  • PMID:22324418
DOID:559 acute pyelonephritis HGNC:6027 Homo sapiens (human) 3579 CXCR2
  • PMID:22325052
DOID:10976 membranous glomerulonephritis HGNC:11740 Homo sapiens (human) 7018 TF
  • PMID:22328173
DOID:9008 psoriatic arthritis HGNC:11365 Homo sapiens (human) 6775 STAT4
  • PMID:22328738
DOID:77 gastrointestinal system disease HGNC:6990 Homo sapiens (human) 4204 MECP2
  • PMID:22331013
DOID:13922 eosinophilic esophagitis HGNC:8823 Homo sapiens (human) 5175 PECAM1
  • PMID:22331014
DOID:1596 depressive disorder HGNC:9031 Homo sapiens (human) 5320 PLA2G2A
  • PMID:22331023
DOID:1070 primary open angle glaucoma HGNC:6922 Homo sapiens (human) 4153 MBL2
  • PMID:22335808
DOID:13378 Kawasaki disease HGNC:320 Homo sapiens (human) 177 AGER
  • PMID:22337222
DOID:1936 atherosclerosis RGD:3656 Rattus norvegicus (Norway rat) 25651 Selp
  • PMID:22340239
DOID:823 periapical periodontitis RGD:2906 Rattus norvegicus (Norway rat) 29385 Cxcr2
  • PMID:22341067
DOID:11555 Fuchs' endothelial dystrophy HGNC:26521 Homo sapiens (human) 125336 LOXHD1
  • PMID:22341973
DOID:12306 vitiligo HGNC:11766 Homo sapiens (human) 7040 TGFB1
  • PMID:22342018
DOID:12306 vitiligo HGNC:5981 Homo sapiens (human) 3605 IL17A
  • PMID:22342018
DOID:12306 vitiligo HGNC:6001 Homo sapiens (human) 3558 IL2
  • PMID:22342018
DOID:12306 vitiligo HGNC:6014 Homo sapiens (human) 3565 IL4
  • PMID:22342018
DOID:0050742 nicotine dependence RGD:2848 Rattus norvegicus (Norway rat) 25187 Htr2c
  • PMID:22342986
DOID:0050908 myelodysplastic syndrome HGNC:23019 Homo sapiens (human) 8233 ZRSR2
  • PMID:22343920
  • PMID:25586593
  • PMID:28220884
  • PMID:28942350
DOID:1612 breast cancer HGNC:9801 Homo sapiens (human) 5879 RAC1
  • PMID:22345078
  • PMID:25557791
DOID:9538 multiple myeloma HGNC:2707 Homo sapiens (human) 1636 ACE
  • PMID:22345095

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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