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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 1351 - 1375 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID ▲ Species Gene ID Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:0060537 mitochondrial complex II deficiency HGNC:10680 Homo sapiens (human) 6389 SDHA
  • MGI:6194238
  • RGD:7240710
DOID:0110435 dilated cardiomyopathy 1GG HGNC:10680 Homo sapiens (human) 6389 SDHA
  • RGD:7240710
DOID:0050700 cardiomyopathy HGNC:10680 Homo sapiens (human) 6389 SDHA
  • MGI:6194238
DOID:10579 leukodystrophy HGNC:10680 Homo sapiens (human) 6389 SDHA
  • MGI:6194238
DOID:3829 pituitary adenoma HGNC:10680 Homo sapiens (human) 6389 SDHA
  • MGI:6194238
DOID:9253 gastrointestinal stromal tumor HGNC:10680 Homo sapiens (human) 6389 SDHA
  • MGI:6194238
DOID:3908 lung non-small cell carcinoma HGNC:10680 Homo sapiens (human) 6389 SDHA
  • PMID:25576295
DOID:0050771 pheochromocytoma HGNC:10680 Homo sapiens (human) 6389 SDHA
  • MGI:6194238
DOID:3652 Leigh disease HGNC:10680 Homo sapiens (human) 6389 SDHA
  • MGI:6194238
  • PMID:7550341
DOID:14330 Parkinson's disease HGNC:10680 Homo sapiens (human) 6389 SDHA
  • PMID:26605748
DOID:0050773 paraganglioma HGNC:10680 Homo sapiens (human) 6389 SDHA
  • MGI:6194238
  • RGD:7240710
DOID:1289 neurodegenerative disease HGNC:10680 Homo sapiens (human) 6389 SDHA
  • MGI:6194238
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
DOID:0050773 paraganglioma HGNC:10681 Homo sapiens (human) 6390 SDHB
  • MGI:6194238
  • PMID:11404820
  • RGD:7240710
DOID:0060537 mitochondrial complex II deficiency HGNC:10681 Homo sapiens (human) 6390 SDHB
  • MGI:6194238
  • RGD:7240710
DOID:9352 type 2 diabetes mellitus HGNC:10681 Homo sapiens (human) 6390 SDHB
  • MGI:6194238
DOID:9253 gastrointestinal stromal tumor HGNC:10681 Homo sapiens (human) 6390 SDHB
  • 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

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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