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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 71001 - 71025 of 71927 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID ▼ Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:4866 salivary gland adenoid cystic carcinoma MGI:2142572 Mus musculus (house mouse) 102103 Mtus1
  • MGI:6194238
DOID:4948 gallbladder carcinoma MGI:2142572 Mus musculus (house mouse) 102103 Mtus1
  • MGI:6194238
DOID:0050865 tongue squamous cell carcinoma MGI:2142572 Mus musculus (house mouse) 102103 Mtus1
  • MGI:6194238
DOID:0111041 glycogen storage disease IXb MGI:97578 Mus musculus (house mouse) 102093 Phkb
  • MGI:6194238
  • PMID:36077341
DOID:0111640 autosomal recessive nonsyndromic deafness 111 HGNC:3496 Homo sapiens (human) 10205 MPZL2
  • RGD:7240710
DOID:3454 brain infarction HGNC:16709 Homo sapiens (human) 10203 CALCRL
  • MGI:6194238
DOID:0050580 hereditary lymphedema HGNC:16709 Homo sapiens (human) 10203 CALCRL
  • RGD:7240710
DOID:8725 vascular dementia HGNC:1774 Homo sapiens (human) 1020 CDK5
  • MGI:6194238
DOID:10652 Alzheimer's disease HGNC:1774 Homo sapiens (human) 1020 CDK5
  • MGI:6194238
  • PMID:15917097
DOID:224 transient cerebral ischemia HGNC:1774 Homo sapiens (human) 1020 CDK5
  • MGI:6194238
DOID:0112231 lissencephaly 7 with cerebellar hypoplasia HGNC:1774 Homo sapiens (human) 1020 CDK5
  • RGD:7240710
DOID:12098 trigeminal neuralgia HGNC:1774 Homo sapiens (human) 1020 CDK5
  • MGI:6194238
DOID:2316 brain ischemia HGNC:1774 Homo sapiens (human) 1020 CDK5
  • MGI:6194238
DOID:1826 epilepsy HGNC:1774 Homo sapiens (human) 1020 CDK5
  • MGI:6194238
DOID:0050453 lissencephaly HGNC:1774 Homo sapiens (human) 1020 CDK5
  • MGI:6194238
DOID:1596 depressive disorder HGNC:1774 Homo sapiens (human) 1020 CDK5
  • MGI:6194238
DOID:9256 colorectal cancer HGNC:188 Homo sapiens (human) 102 ADAM10
  • PMID:31565100
DOID:10652 Alzheimer's disease HGNC:188 Homo sapiens (human) 102 ADAM10
  • MGI:6194238
DOID:0081292 traumatic brain injury HGNC:188 Homo sapiens (human) 102 ADAM10
  • MGI:6194238
DOID:83 cataract HGNC:188 Homo sapiens (human) 102 ADAM10
  • MGI:6194238
DOID:0050700 cardiomyopathy HGNC:188 Homo sapiens (human) 102 ADAM10
  • MGI:6194238
DOID:0060258 reticulate acropigmentation of Kitamura HGNC:188 Homo sapiens (human) 102 ADAM10
  • RGD:7240710
DOID:14004 thoracic aortic aneurysm HGNC:188 Homo sapiens (human) 102 ADAM10
  • MGI:6194238
DOID:0110050 Alzheimer's disease 18 HGNC:188 Homo sapiens (human) 102 ADAM10
  • RGD:7240710
DOID:1824 status epilepticus HGNC:188 Homo sapiens (human) 102 ADAM10
  • MGI:6194238

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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: December 9, 2024