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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 4551 - 4575 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID ▲ Species Gene ID Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:0111352 D-2-hydroxyglutaric aciduria 2 HGNC:5383 Homo sapiens (human) 3418 IDH2
  • RGD:7240710
DOID:3910 lung adenocarcinoma HGNC:5383 Homo sapiens (human) 3418 IDH2
  • PMID:29465809
  • PMID:30128035
DOID:3907 lung squamous cell carcinoma HGNC:5383 Homo sapiens (human) 3418 IDH2
  • PMID:27649069
  • PMID:29465809
  • PMID:30128035
DOID:4928 intrahepatic cholangiocarcinoma HGNC:5383 Homo sapiens (human) 3418 IDH2
  • PMID:22824796
DOID:0112147 retinitis pigmentosa 90 HGNC:5384 Homo sapiens (human) 3419 IDH3A
  • RGD:7240710
DOID:439 neuromuscular junction disease HGNC:5384 Homo sapiens (human) 3419 IDH3A
  • MGI:6194238
DOID:0050709 early infantile epileptic encephalopathy HGNC:5384 Homo sapiens (human) 3419 IDH3A
  • MGI:6194238
DOID:0110409 retinitis pigmentosa 46 HGNC:5385 Homo sapiens (human) 3420 IDH3B
  • RGD:7240710
DOID:0050709 early infantile epileptic encephalopathy HGNC:5385 Homo sapiens (human) 3420 IDH3B
  • MGI:6194238
DOID:0050709 early infantile epileptic encephalopathy HGNC:5386 Homo sapiens (human) 3421 IDH3G
  • MGI:6194238
DOID:12799 mucopolysaccharidosis II HGNC:5389 Homo sapiens (human) 3423 IDS
  • MGI:6194238
  • PMID:1550586
  • PMID:27146977
  • RGD:7240710
DOID:12802 mucopolysaccharidosis I HGNC:5391 Homo sapiens (human) 3425 IDUA
  • MGI:6194238
  • PMID:11172140
  • PMID:12948739
  • PMID:1301196
  • PMID:1301941
  • PMID:15126990
  • PMID:15128896
  • PMID:15194053
  • PMID:16435195
  • PMID:16860035
  • PMID:17407189
  • PMID:17606547
  • PMID:18523448
  • PMID:21734815
  • PMID:24100243
  • PMID:25597593
  • PMID:27146977
  • PMID:7951228
  • PMID:8664897
DOID:0111390 mucopolysaccharidosis Ih HGNC:5391 Homo sapiens (human) 3425 IDUA
  • RGD:7240710
DOID:0111389 mucopolysaccharidosis Ih/s HGNC:5391 Homo sapiens (human) 3425 IDUA
  • RGD:7240710
DOID:10754 otitis media HGNC:5391 Homo sapiens (human) 3425 IDUA
  • MGI:6194238
DOID:10808 gastric ulcer HGNC:5391 Homo sapiens (human) 3425 IDUA
  • MGI:6194238
DOID:0060222 Scheie syndrome HGNC:5391 Homo sapiens (human) 3425 IDUA
  • RGD:7240710
DOID:0081312 T-cell non-Hodgkin lymphoma HGNC:5392 Homo sapiens (human) 8870 IER3
  • PMID:14534530
DOID:10873 Kuhnt-Junius degeneration HGNC:543 Homo sapiens (human) 308 ANXA5
  • PMID:19684010
DOID:2921 glomerulonephritis HGNC:543 Homo sapiens (human) 308 ANXA5
  • MGI:6194238
DOID:14330 Parkinson's disease HGNC:543 Homo sapiens (human) 308 ANXA5
  • PMID:10584677
DOID:1459 hypothyroidism HGNC:543 Homo sapiens (human) 308 ANXA5
  • MGI:6194238
DOID:11383 cryptorchidism HGNC:543 Homo sapiens (human) 308 ANXA5
  • MGI:6194238
DOID:893 Wilson disease HGNC:543 Homo sapiens (human) 308 ANXA5
  • MGI:6194238
DOID:10652 Alzheimer's disease HGNC:543 Homo sapiens (human) 308 ANXA5
  • PMID:20648654

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GlyCosmos is a member of the GlySpace Alliance together with GlyGen and Glycomics@ExPASy.

Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

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


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