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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 401 - 425 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB Evidence Code Names ▼ References
DOID:10783 methemoglobinemia HGNC:2873 Homo sapiens (human) 1727 CYB5R3
  • PMID:11295830
DOID:446 primary hyperaldosteronism HGNC:2591 Homo sapiens (human) 1584 CYP11B1
  • PMID:1731223
DOID:8947 diabetic retinopathy HGNC:288 Homo sapiens (human) 155 ADRB3
  • PMID:9313761
DOID:12804 mucopolysaccharidosis IV HGNC:4298 Homo sapiens (human) 2720 GLB1
  • PMID:11511921
  • PMID:19091613
DOID:3211 lysosomal storage disease HGNC:318 Homo sapiens (human) 175 AGA
  • PMID:1703489
DOID:0070112 Niemann-Pick disease type B HGNC:11120 Homo sapiens (human) 6609 SMPD1
  • RGD:7240710
DOID:11713 diabetic angiopathy HGNC:11892 Homo sapiens (human) 7124 TNF
  • PMID:18575614
DOID:4483 rhinitis HGNC:1628 Homo sapiens (human) 929 CD14
  • PMID:16950285
  • PMID:20109306
DOID:0112303 spondylometaphyseal dysplasia with corneal dystrophy HGNC:9056 Homo sapiens (human) 5331 PLCB3
  • RGD:7240710
DOID:2394 ovarian cancer HGNC:8125 Homo sapiens (human) 4968 OGG1
  • PMID:24698998
DOID:0050860 colorectal adenoma HGNC:9603 Homo sapiens (human) 5740 PTGIS
  • PMID:16537708
DOID:552 pneumonia HGNC:79 Homo sapiens (human) 28 ABO
  • PMID:4375858
DOID:0050589 inflammatory bowel disease HGNC:5344 Homo sapiens (human) 3383 ICAM1
  • PMID:15638228
DOID:848 arthritis HGNC:270 Homo sapiens (human) 142 PARP1
  • PMID:16461442
DOID:5844 myocardial infarction HGNC:6562 Homo sapiens (human) 3957 LGALS2
  • PMID:15129282
  • RGD:7240710
DOID:0080199 colorectal carcinoma HGNC:11998 Homo sapiens (human) 7157 TP53
  • PMID:29560751
DOID:4247 coronary restenosis HGNC:11998 Homo sapiens (human) 7157 TP53
  • PMID:14740296
DOID:0112361 spondylocostal dysostosis 3 HGNC:6560 Homo sapiens (human) 3955 LFNG
  • RGD:7240710
DOID:0070352 stress-induced childhood-onset neurodegeneration with variable ataxia and seizures HGNC:21304 Homo sapiens (human) 54936 ADPRS
  • RGD:7240710
DOID:1287 cardiovascular system disease HGNC:6623 Homo sapiens (human) 9388 LIPG
  • PMID:16023652
DOID:0080582 hypotrichosis 14 HGNC:6708 Homo sapiens (human) 4047 LSS
  • RGD:7240710
DOID:0060326 myelomeningocele HGNC:11005 Homo sapiens (human) 6513 SLC2A1
  • PMID:21135204
  • PMID:23427181
DOID:5016 hepatocellular clear cell carcinoma HGNC:5383 Homo sapiens (human) 3418 IDH2
  • PMID:25355558
DOID:10584 retinitis pigmentosa HGNC:19139 Homo sapiens (human) 55624 POMGNT1
  • RGD:7240710
DOID:0080626 corticosterone methyloxidase deficiency 1 HGNC:2592 Homo sapiens (human) 1585 CYP11B2
  • RGD:7240710

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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