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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 6251 - 6275 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID Species ▼ Gene ID Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:0050866 oral squamous cell carcinoma HGNC:4617 Homo sapiens (human) 2932 GSK3B
  • PMID:21393552
DOID:10763 hypertension HGNC:404 Homo sapiens (human) 217 ALDH2
  • PMID:11510748
  • PMID:12484509
DOID:9744 type 1 diabetes mellitus HGNC:2606 Homo sapiens (human) 1594 CYP27B1
  • PMID:17223345
  • PMID:17606874
DOID:1067 open-angle glaucoma HGNC:11892 Homo sapiens (human) 7124 TNF
  • PMID:20357201
DOID:4194 glucose metabolism disease HGNC:6126 Homo sapiens (human) 8660 IRS2
  • MGI:6194238
DOID:784 chronic kidney disease HGNC:2843 Homo sapiens (human) 8694 DGAT1
  • MGI:6194238
DOID:2349 arteriosclerosis HGNC:9605 Homo sapiens (human) 5743 PTGS2
  • PMID:16458279
DOID:0081312 T-cell non-Hodgkin lymphoma HGNC:5392 Homo sapiens (human) 8870 IER3
  • PMID:14534530
DOID:4029 gastritis HGNC:9605 Homo sapiens (human) 5743 PTGS2
  • MGI:6194238
DOID:9352 type 2 diabetes mellitus HGNC:5467 Homo sapiens (human) 3482 IGF2R
  • PMID:16868148
DOID:783 end stage renal disease HGNC:11892 Homo sapiens (human) 7124 TNF
  • PMID:22266663
DOID:2999 granulosa cell tumor HGNC:9605 Homo sapiens (human) 5743 PTGS2
  • PMID:11994539
DOID:224 transient cerebral ischemia HGNC:4555 Homo sapiens (human) 2878 GPX3
  • PMID:30098076
DOID:13317 hyperinsulinemic hypoglycemia HGNC:4195 Homo sapiens (human) 2645 GCK
  • MGI:6194238
DOID:1574 alcohol use disorder HGNC:90 Homo sapiens (human) 35 ACADS
  • PMID:20554694
DOID:6432 pulmonary hypertension HGNC:9603 Homo sapiens (human) 5740 PTGIS
  • MGI:6194238
  • PMID:12019369
  • PMID:32673988
DOID:0060060 non-Hodgkin lymphoma HGNC:5344 Homo sapiens (human) 3383 ICAM1
  • PMID:7686390
DOID:0110429 dilated cardiomyopathy 1H HGNC:288 Homo sapiens (human) 155 ADRB3
  • PMID:20123316
DOID:9351 diabetes mellitus HGNC:4195 Homo sapiens (human) 2645 GCK
  • PMID:11372010
DOID:1168 familial hyperlipidemia HGNC:6522 Homo sapiens (human) 3931 LCAT
  • MGI:6194238
DOID:4450 renal cell carcinoma HGNC:2595 Homo sapiens (human) 1543 CYP1A1
  • MGI:6194238
  • PMID:22000673
  • PMID:22296350
  • PMID:9631944
DOID:4195 hyperglycemia HGNC:10658 Homo sapiens (human) 6382 SDC1
  • PMID:16810465
DOID:10783 methemoglobinemia HGNC:2873 Homo sapiens (human) 1727 CYB5R3
  • PMID:11295830
DOID:9074 systemic lupus erythematosus HGNC:6824 Homo sapiens (human) 4124 MAN2A1
  • MGI:6194238
DOID:446 primary hyperaldosteronism HGNC:2591 Homo sapiens (human) 1584 CYP11B1
  • PMID:1731223

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Supported by JST NBDC Grant Number JPMJND2204

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


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