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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 4251 - 4275 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol ▼ FlyGlycoDB Evidence Code Names References
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:104 bacterial infectious disease HGNC:10661 Homo sapiens (human) 6385 SDC4
  • MGI:6194238
DOID:5844 myocardial infarction HGNC:10661 Homo sapiens (human) 6385 SDC4
  • PMID:11372670
DOID:9970 obesity HGNC:10660 Homo sapiens (human) 9672 SDC3
  • RGD:7240710
DOID:674 cleft palate HGNC:10659 Homo sapiens (human) 6383 SDC2
  • PMID:18716610
DOID:9352 type 2 diabetes mellitus HGNC:10659 Homo sapiens (human) 6383 SDC2
  • PMID:14976204
DOID:9296 cleft lip HGNC:10659 Homo sapiens (human) 6383 SDC2
  • PMID:18716610
DOID:9970 obesity HGNC:10658 Homo sapiens (human) 6382 SDC1
  • MGI:6194238
DOID:4195 hyperglycemia HGNC:10658 Homo sapiens (human) 6382 SDC1
  • PMID:16810465
DOID:1168 familial hyperlipidemia HGNC:10658 Homo sapiens (human) 6382 SDC1
  • MGI:6194238
DOID:8567 Hodgkin's lymphoma HGNC:10658 Homo sapiens (human) 6382 SDC1
  • PMID:9746758
DOID:576 proteinuria HGNC:10658 Homo sapiens (human) 6382 SDC1
  • MGI:6194238
DOID:5844 myocardial infarction HGNC:10658 Homo sapiens (human) 6382 SDC1
  • MGI:6194238
DOID:3910 lung adenocarcinoma HGNC:10658 Homo sapiens (human) 6382 SDC1
  • PMID:23374247
DOID:9970 obesity HGNC:10606 Homo sapiens (human) 6342 SCP2
  • MGI:6194238
DOID:905 Zellweger syndrome HGNC:10606 Homo sapiens (human) 6342 SCP2
  • PMID:3555624

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Supported by JST NBDC Grant Number JPMJND2204

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Last updated: August 19, 2024