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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 3976 - 4000 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID ▲ Species Gene ID Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:9351 diabetes mellitus HGNC:4195 Homo sapiens (human) 2645 GCK
  • PMID:11372010
DOID:0111100 maturity-onset diabetes of the young type 2 HGNC:4195 Homo sapiens (human) 2645 GCK
  • MGI:6194238
  • RGD:7240710
DOID:9352 type 2 diabetes mellitus HGNC:4195 Homo sapiens (human) 2645 GCK
  • MGI:6194238
  • PMID:1570017
  • PMID:8200206
  • PMID:8314445
  • PMID:8325445
  • RGD:7240710
DOID:0070216 familial hyperinsulinemic hypoglycemia 3 HGNC:4195 Homo sapiens (human) 2645 GCK
  • MGI:6194238
  • RGD:7240710
DOID:10763 hypertension HGNC:4195 Homo sapiens (human) 2645 GCK
  • PMID:9324112
DOID:2018 hyperinsulinism HGNC:4195 Homo sapiens (human) 2645 GCK
  • PMID:9435328
DOID:3393 coronary artery disease HGNC:4195 Homo sapiens (human) 2645 GCK
  • PMID:15173029
DOID:0060639 permanent neonatal diabetes mellitus HGNC:4195 Homo sapiens (human) 2645 GCK
  • RGD:7240710
DOID:9452 steatotic liver disease HGNC:4195 Homo sapiens (human) 2645 GCK
  • MGI:6194238
DOID:4195 hyperglycemia HGNC:4195 Homo sapiens (human) 2645 GCK
  • MGI:6194238
DOID:0050524 maturity-onset diabetes of the young HGNC:4195 Homo sapiens (human) 2645 GCK
  • MGI:6194238
DOID:4194 glucose metabolism disease HGNC:4195 Homo sapiens (human) 2645 GCK
  • MGI:6194238
DOID:9970 obesity HGNC:4195 Homo sapiens (human) 2645 GCK
  • MGI:6194238
DOID:9993 hypoglycemia HGNC:4195 Homo sapiens (human) 2645 GCK
  • PMID:9435328
DOID:557 kidney disease HGNC:4201 Homo sapiens (human) 2648 KAT2A
  • MGI:6194238
DOID:3908 lung non-small cell carcinoma HGNC:4201 Homo sapiens (human) 2648 KAT2A
  • PMID:23543735
DOID:114 heart disease HGNC:4201 Homo sapiens (human) 2648 KAT2A
  • MGI:6194238
DOID:0110242 cataract 13 with adult i phenotype HGNC:4204 Homo sapiens (human) 2651 GCNT2
  • RGD:7240710
DOID:83 cataract HGNC:4204 Homo sapiens (human) 2651 GCNT2
  • PMID:15161861
DOID:0070330 multiple mitochondrial dysfunctions syndrome HGNC:4208 Homo sapiens (human) 2653 GCSH
  • RGD:7240710
DOID:9268 glycine encephalopathy HGNC:4208 Homo sapiens (human) 2653 GCSH
  • MGI:6194238
DOID:9252 amino acid metabolic disorder HGNC:4208 Homo sapiens (human) 2653 GCSH
  • PMID:7070876
DOID:1168 familial hyperlipidemia HGNC:4241 Homo sapiens (human) 2673 GFPT1
  • MGI:6194238
DOID:9970 obesity HGNC:4241 Homo sapiens (human) 2673 GFPT1
  • PMID:11118009
DOID:9352 type 2 diabetes mellitus HGNC:4241 Homo sapiens (human) 2673 GFPT1
  • PMID:17574229

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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