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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 July 29, 2024
Displaying entries 10826 - 10850 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID ▼ Species Gene ID Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:0060180 colitis HGNC:10720 Homo sapiens (human) 6402 SELL
  • MGI:6194238
DOID:289 endometriosis HGNC:10720 Homo sapiens (human) 6402 SELL
  • MGI:6194238
DOID:9744 type 1 diabetes mellitus HGNC:10720 Homo sapiens (human) 6402 SELL
  • MGI:6194238
DOID:9074 systemic lupus erythematosus HGNC:10720 Homo sapiens (human) 6402 SELL
  • PMID:20512127
DOID:0081267 graft-versus-host disease HGNC:10720 Homo sapiens (human) 6402 SELL
  • PMID:21635226
DOID:2316 brain ischemia HGNC:10718 Homo sapiens (human) 6401 SELE
  • PMID:19107136
DOID:6713 cerebrovascular disease HGNC:10718 Homo sapiens (human) 6401 SELE
  • PMID:16843446
DOID:9744 type 1 diabetes mellitus HGNC:10718 Homo sapiens (human) 6401 SELE
  • PMID:18791689
DOID:0080600 COVID-19 HGNC:10718 Homo sapiens (human) 6401 SELE
  • PMID:32458111
DOID:3393 coronary artery disease HGNC:10718 Homo sapiens (human) 6401 SELE
  • PMID:17578587
DOID:2986 IgA glomerulonephritis HGNC:10718 Homo sapiens (human) 6401 SELE
  • PMID:11828340
DOID:8481 rheumatic myocarditis HGNC:10718 Homo sapiens (human) 6401 SELE
  • PMID:22987107
DOID:0080533 Carney-Stratakis syndrome HGNC:10683 Homo sapiens (human) 6392 SDHD
  • RGD:7240710
DOID:0050773 paraganglioma HGNC:10683 Homo sapiens (human) 6392 SDHD
  • MGI:6194238
  • PMID:10657297
  • RGD:7240710
DOID:11984 hypertrophic cardiomyopathy HGNC:10683 Homo sapiens (human) 6392 SDHD
  • MGI:6194238
DOID:0060537 mitochondrial complex II deficiency HGNC:10683 Homo sapiens (human) 6392 SDHD
  • MGI:6194238
  • RGD:7240710
DOID:9253 gastrointestinal stromal tumor HGNC:10682 Homo sapiens (human) 6391 SDHC
  • RGD:7240710
DOID:3652 Leigh disease HGNC:10682 Homo sapiens (human) 6391 SDHC
  • MGI:6194238
DOID:0050773 paraganglioma HGNC:10682 Homo sapiens (human) 6391 SDHC
  • PMID:11062460
  • RGD:7240710
DOID:0080533 Carney-Stratakis syndrome HGNC:10682 Homo sapiens (human) 6391 SDHC
  • RGD:7240710
DOID:3908 lung non-small cell carcinoma HGNC:10682 Homo sapiens (human) 6391 SDHC
  • PMID:25576295
DOID:0050771 pheochromocytoma HGNC:10681 Homo sapiens (human) 6390 SDHB
  • PMID:11404820
DOID:9408 acute myocardial infarction HGNC:10681 Homo sapiens (human) 6390 SDHB
  • MGI:6194238
DOID:890 mitochondrial encephalomyopathy HGNC:10681 Homo sapiens (human) 6390 SDHB
  • MGI:6194238
DOID:0080533 Carney-Stratakis syndrome HGNC:10681 Homo sapiens (human) 6390 SDHB
  • RGD:7240710

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Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01


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Last updated: August 19, 2024