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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 3876 - 3900 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol ▲ FlyGlycoDB Evidence Code Names References
DOID:9952 acute lymphoblastic leukemia HGNC:4922 Homo sapiens (human) 3098 HK1
  • PMID:21921332
DOID:6432 pulmonary hypertension HGNC:4922 Homo sapiens (human) 3098 HK1
  • MGI:6194238
DOID:10923 sickle cell anemia HGNC:4922 Homo sapiens (human) 3098 HK1
  • PMID:5686464
DOID:9256 colorectal cancer HGNC:4922 Homo sapiens (human) 3098 HK1
  • MGI:6194238
DOID:9352 type 2 diabetes mellitus HGNC:4923 Homo sapiens (human) 3099 HK2
  • PMID:11319725
DOID:0050524 maturity-onset diabetes of the young HGNC:4923 Homo sapiens (human) 3099 HK2
  • MGI:6194238
DOID:10763 hypertension HGNC:4923 Homo sapiens (human) 3099 HK2
  • MGI:6194238
DOID:9970 obesity HGNC:4923 Homo sapiens (human) 3099 HK2
  • MGI:6194238
  • PMID:11319725
DOID:13317 hyperinsulinemic hypoglycemia HGNC:4923 Homo sapiens (human) 3099 HK2
  • MGI:6194238
DOID:4195 hyperglycemia HGNC:4923 Homo sapiens (human) 3099 HK2
  • MGI:6194238
DOID:4194 glucose metabolism disease HGNC:4923 Homo sapiens (human) 3099 HK2
  • MGI:6194238
DOID:13317 hyperinsulinemic hypoglycemia HGNC:4925 Homo sapiens (human) 3101 HK3
  • MGI:6194238
DOID:0050524 maturity-onset diabetes of the young HGNC:4925 Homo sapiens (human) 3101 HK3
  • MGI:6194238
DOID:4195 hyperglycemia HGNC:4925 Homo sapiens (human) 3101 HK3
  • MGI:6194238
DOID:4194 glucose metabolism disease HGNC:4925 Homo sapiens (human) 3101 HK3
  • MGI:6194238
DOID:4194 glucose metabolism disease HGNC:23302 Homo sapiens (human) 80201 HKDC1
  • MGI:6194238
DOID:4195 hyperglycemia HGNC:23302 Homo sapiens (human) 80201 HKDC1
  • MGI:6194238
DOID:13317 hyperinsulinemic hypoglycemia HGNC:23302 Homo sapiens (human) 80201 HKDC1
  • MGI:6194238
DOID:0050524 maturity-onset diabetes of the young HGNC:23302 Homo sapiens (human) 80201 HKDC1
  • MGI:6194238
DOID:10584 retinitis pigmentosa HGNC:23302 Homo sapiens (human) 80201 HKDC1
  • RGD:7240710
DOID:9252 amino acid metabolic disorder HGNC:5005 Homo sapiens (human) 3155 HMGCL
  • PMID:8440722
DOID:9970 obesity HGNC:5007 Homo sapiens (human) 3157 HMGCS1
  • MGI:6194238
DOID:13619 extrahepatic cholestasis HGNC:5008 Homo sapiens (human) 3158 HMGCS2
  • MGI:6194238
DOID:0081168 HMG-CoA synthase 2 deficiency HGNC:5008 Homo sapiens (human) 3158 HMGCS2
  • MGI:6194238
  • RGD:7240710
DOID:684 hepatocellular carcinoma HGNC:5008 Homo sapiens (human) 3158 HMGCS2
  • PMID:28867541

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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