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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 3301 - 3325 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID Species ▲ Gene ID Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:9256 colorectal cancer HGNC:4311 Homo sapiens (human) 2729 GCLC
  • PMID:8705999
DOID:397 restrictive cardiomyopathy HGNC:10571 Homo sapiens (human) 6319 SCD
  • MGI:6194238
DOID:13544 low tension glaucoma HGNC:11850 Homo sapiens (human) 7099 TLR4
  • PMID:21921986
  • PMID:22831837
DOID:4483 rhinitis HGNC:6553 Homo sapiens (human) 3952 LEP
  • PMID:19860581
DOID:12858 Huntington's disease HGNC:108 Homo sapiens (human) 43 ACHE
  • PMID:2953866
DOID:0081097 Rafiq syndrome HGNC:6823 Homo sapiens (human) 11253 MAN1B1
  • RGD:7240710
DOID:0080552 congenital disorder of glycosylation Ia HGNC:9114 Homo sapiens (human) 5372 PMM1
  • MGI:6194238
DOID:5577 gastrinoma HGNC:11006 Homo sapiens (human) 6514 SLC2A2
  • PMID:12114701
  • PMID:8421107
DOID:11714 gestational diabetes HGNC:20580 Homo sapiens (human) 120227 CYP2R1
  • PMID:36477942
DOID:2018 hyperinsulinism HGNC:13633 Homo sapiens (human) 9370 ADIPOQ
  • MGI:6194238
DOID:14499 Fabry disease HGNC:4296 Homo sapiens (human) 2717 GLA
  • MGI:6194238
  • PMID:2539398
  • RGD:7240710
DOID:6000 congestive heart failure HGNC:270 Homo sapiens (human) 142 PARP1
  • MGI:6194238
DOID:1485 cystic fibrosis HGNC:2595 Homo sapiens (human) 1543 CYP1A1
  • PMID:14593914
DOID:3770 pulmonary fibrosis HGNC:1932 Homo sapiens (human) 1116 CHI3L1
  • PMID:20888745
DOID:9352 type 2 diabetes mellitus HGNC:9053 Homo sapiens (human) 5329 PLAUR
  • PMID:22050462
DOID:4947 cholangiocarcinoma HGNC:8125 Homo sapiens (human) 4968 OGG1
  • PMID:11260864
  • PMID:11866974
DOID:0112251 Ghosal hematodiaphyseal syndrome HGNC:11609 Homo sapiens (human) 6916 TBXAS1
  • RGD:7240710
DOID:0111100 maturity-onset diabetes of the young type 2 HGNC:4195 Homo sapiens (human) 2645 GCK
  • MGI:6194238
  • RGD:7240710
DOID:3525 middle cerebral artery infarction HGNC:4819 Homo sapiens (human) 3037 HAS2
  • MGI:6194238
DOID:1936 atherosclerosis HGNC:9603 Homo sapiens (human) 5740 PTGIS
  • PMID:22112851
DOID:0050570 congenital disorder of glycosylation type I HGNC:25812 Homo sapiens (human) 79644 SRD5A3
  • MGI:6194238
DOID:3021 acute kidney failure HGNC:936 Homo sapiens (human) 572 BAD
  • MGI:6194238
DOID:0111933 phosphoglycerate kinase 1 deficiency HGNC:8896 Homo sapiens (human) 5230 PGK1
  • RGD:7240710
DOID:5434 scrapie HGNC:9449 Homo sapiens (human) 5621 PRNP
  • MGI:6194238
DOID:3908 lung non-small cell carcinoma HGNC:5195 Homo sapiens (human) 9956 HS3ST2
  • PMID:27777637

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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