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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 2651 - 2675 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID ▼ Gene Symbol FlyGlycoDB Evidence Code Names References
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:0050628 advanced sleep phase syndrome RGD:61945 Rattus norvegicus (Norway rat) 63840 Per2
  • MGI:6194238
DOID:9975 cocaine dependence RGD:61945 Rattus norvegicus (Norway rat) 63840 Per2
  • MGI:6194238
DOID:0110011 advanced sleep phase syndrome 1 RGD:61945 Rattus norvegicus (Norway rat) 63840 Per2
  • MGI:6194238
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:10584 retinitis pigmentosa HGNC:23059 Homo sapiens (human) 63827 BCAN
  • PMID:29150673
DOID:3525 middle cerebral artery infarction HGNC:23059 Homo sapiens (human) 63827 BCAN
  • MGI:6194238
DOID:3070 high grade glioma HGNC:23059 Homo sapiens (human) 63827 BCAN
  • MGI:6194238
  • PMID:16061654
  • PMID:23253190
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

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


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Last updated: August 19, 2024