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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 October 9, 2024
Displaying entries 70601 - 70625 of 71927 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID ▼ Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:12858 Huntington's disease MGI:2145955 Mus musculus (house mouse) 105787 Prkaa1
  • MGI:6194238
DOID:3908 lung non-small cell carcinoma MGI:2145955 Mus musculus (house mouse) 105787 Prkaa1
  • MGI:6194238
DOID:9352 type 2 diabetes mellitus MGI:2145955 Mus musculus (house mouse) 105787 Prkaa1
  • MGI:6194238
DOID:219 colon cancer MGI:2145955 Mus musculus (house mouse) 105787 Prkaa1
  • MGI:6194238
DOID:9970 obesity MGI:2145955 Mus musculus (house mouse) 105787 Prkaa1
  • MGI:6194238
DOID:13580 cholestasis MGI:2145955 Mus musculus (house mouse) 105787 Prkaa1
  • MGI:6194238
DOID:0070114 Niemann-Pick disease type C2 HGNC:14537 Homo sapiens (human) 10577 NPC2
  • RGD:7240710
DOID:14504 Niemann-Pick disease HGNC:14537 Homo sapiens (human) 10577 NPC2
  • MGI:6194238
  • PMID:11567215
DOID:1508 candidiasis HGNC:1615 Homo sapiens (human) 10576 CCT2
  • MGI:6194238
DOID:14791 Leber congenital amaurosis HGNC:1615 Homo sapiens (human) 10576 CCT2
  • MGI:6194238
DOID:0060036 intrinsic cardiomyopathy HGNC:1617 Homo sapiens (human) 10575 CCT4
  • MGI:6194238
DOID:0050548 hereditary sensory neuropathy HGNC:1617 Homo sapiens (human) 10575 CCT4
  • MGI:6194238
DOID:0110055 amelogenesis imperfecta type 3A MGI:2145900 Mus musculus (house mouse) 105732 Fam83h
  • MGI:6194238
DOID:11832 visual epilepsy MGI:2145895 Mus musculus (house mouse) 105727 Slc38a1
  • MGI:6194238
DOID:684 hepatocellular carcinoma MGI:2145895 Mus musculus (house mouse) 105727 Slc38a1
  • MGI:6194238
DOID:0111052 Scott syndrome MGI:2145890 Mus musculus (house mouse) 105722 Ano6
  • MGI:6194238
DOID:0050589 inflammatory bowel disease MGI:2145890 Mus musculus (house mouse) 105722 Ano6
  • MGI:6194238
DOID:7147 ankylosing spondylitis MGI:2145890 Mus musculus (house mouse) 105722 Ano6
  • MGI:6194238
DOID:936 brain disease MGI:2179432 Mus musculus (house mouse) 105689 Mycbp2
  • MGI:6194238
DOID:12117 pulmonary alveolar microlithiasis HGNC:11020 Homo sapiens (human) 10568 SLC34A2
  • RGD:7240710
DOID:0050454 periventricular nodular heterotopia HGNC:15853 Homo sapiens (human) 10564 ARFGEF2
  • PMID:14647276
  • RGD:7240710
DOID:0090117 thiamine-responsive megaloblastic anemia syndrome HGNC:10938 Homo sapiens (human) 10560 SLC19A2
  • MGI:6194238
  • RGD:7240710
DOID:13382 megaloblastic anemia HGNC:10938 Homo sapiens (human) 10560 SLC19A2
  • PMID:10391221
DOID:9351 diabetes mellitus HGNC:10938 Homo sapiens (human) 10560 SLC19A2
  • PMID:10391221
DOID:784 chronic kidney disease HGNC:10938 Homo sapiens (human) 10560 SLC19A2
  • MGI:6194238

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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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Last updated: December 9, 2024