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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 1076 - 1100 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID ▲ Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:8466 retinal degeneration MGI:88529 Mus musculus (house mouse) 12974 Cs
  • MGI:6194238
DOID:0050852 limb ischemia MGI:88529 Mus musculus (house mouse) 12974 Cs
  • MGI:6194238
DOID:11984 hypertrophic cardiomyopathy MGI:88529 Mus musculus (house mouse) 12974 Cs
  • MGI:6194238
DOID:12930 dilated cardiomyopathy MGI:88529 Mus musculus (house mouse) 12974 Cs
  • MGI:6194238
DOID:5844 myocardial infarction MGI:88529 Mus musculus (house mouse) 12974 Cs
  • MGI:6194238
DOID:7998 hyperthyroidism MGI:88529 Mus musculus (house mouse) 12974 Cs
  • MGI:6194238
DOID:6000 congestive heart failure MGI:88529 Mus musculus (house mouse) 12974 Cs
  • MGI:6194238
DOID:1459 hypothyroidism MGI:88529 Mus musculus (house mouse) 12974 Cs
  • MGI:6194238
DOID:2256 osteochondrodysplasia HGNC:2218 Homo sapiens (human) 1298 COL9A2
  • PMID:8528240
DOID:0080046 Stickler syndrome HGNC:2218 Homo sapiens (human) 1298 COL9A2
  • RGD:7240710
DOID:0070298 multiple epiphyseal dysplasia 2 HGNC:2218 Homo sapiens (human) 1298 COL9A2
  • RGD:7240710
DOID:11446 sciatic neuropathy HGNC:29595 Homo sapiens (human) 130120 REG3G
  • MGI:6194238
DOID:11832 visual epilepsy HGNC:29595 Homo sapiens (human) 130120 REG3G
  • MGI:6194238
DOID:552 pneumonia HGNC:29595 Homo sapiens (human) 130120 REG3G
  • MGI:6194238
DOID:2913 acute pancreatitis HGNC:29595 Homo sapiens (human) 130120 REG3G
  • MGI:6194238
DOID:9352 type 2 diabetes mellitus HGNC:29595 Homo sapiens (human) 130120 REG3G
  • MGI:6194238
DOID:9870 galactosemia HGNC:24063 Homo sapiens (human) 130589 GALM
  • RGD:7240710
DOID:14330 Parkinson's disease HGNC:256 Homo sapiens (human) 131 ADH7
  • MGI:6194238
DOID:10763 hypertension HGNC:2228 Homo sapiens (human) 1312 COMT
  • MGI:6194238
  • PMID:17143180
DOID:1574 alcohol use disorder HGNC:2228 Homo sapiens (human) 1312 COMT
  • PMID:10395222
  • PMID:32889058
DOID:12306 vitiligo HGNC:2228 Homo sapiens (human) 1312 COMT
  • PMID:19112571
  • PMID:24915010
DOID:1612 breast cancer HGNC:2228 Homo sapiens (human) 1312 COMT
  • PMID:15285606
  • PMID:17429315
  • PMID:17507616
  • PMID:17562079
DOID:11612 polycystic ovary syndrome HGNC:2228 Homo sapiens (human) 1312 COMT
  • PMID:17535988
DOID:0060041 autism spectrum disorder HGNC:2228 Homo sapiens (human) 1312 COMT
  • PMID:25325218
DOID:4450 renal cell carcinoma HGNC:2228 Homo sapiens (human) 1312 COMT
  • PMID:17220335

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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