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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 71076 - 71100 of 71927 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID ▼ Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:14330 Parkinson's disease HGNC:17142 Homo sapiens (human) 10133 OPTN
  • MGI:6194238
DOID:0081294 neuronal intranuclear inclusion disease HGNC:17142 Homo sapiens (human) 10133 OPTN
  • PMID:22318854
DOID:13544 low tension glaucoma HGNC:17142 Homo sapiens (human) 10133 OPTN
  • MGI:6194238
  • PMID:15226658
  • PMID:15557444
  • PMID:16148883
DOID:1686 glaucoma HGNC:17142 Homo sapiens (human) 10133 OPTN
  • PMID:16148883
DOID:12858 Huntington's disease HGNC:17142 Homo sapiens (human) 10133 OPTN
  • PMID:22318854
DOID:13948 bladder neck obstruction HGNC:17142 Homo sapiens (human) 10133 OPTN
  • MGI:6194238
DOID:1067 open-angle glaucoma HGNC:17142 Homo sapiens (human) 10133 OPTN
  • PMID:11834836
  • PMID:14627677
  • PMID:16020311
  • PMID:19096531
DOID:5408 Paget's disease of bone HGNC:17142 Homo sapiens (human) 10133 OPTN
  • PMID:20436471
DOID:1070 primary open angle glaucoma HGNC:17142 Homo sapiens (human) 10133 OPTN
  • PMID:15226658
  • PMID:15557444
  • PMID:19172505
  • RGD:7240710
DOID:576 proteinuria HGNC:17142 Homo sapiens (human) 10133 OPTN
  • MGI:6194238
DOID:0070033 autosomal dominant intellectual developmental disorder 3 HGNC:1754 Homo sapiens (human) 1013 CDH15
  • RGD:7240710
DOID:0050888 syndromic intellectual disability HGNC:20367 Homo sapiens (human) 10129 FRY
  • MGI:6194238
DOID:0111180 French Canadian Leigh disease HGNC:15714 Homo sapiens (human) 10128 LRPPRC
  • RGD:7240710
DOID:3652 Leigh disease HGNC:15714 Homo sapiens (human) 10128 LRPPRC
  • PMID:12529507
DOID:14250 Down syndrome HGNC:167 Homo sapiens (human) 10121 ACTR1A
  • PMID:11829462
DOID:219 colon cancer HGNC:167 Homo sapiens (human) 10121 ACTR1A
  • PMID:26422100
DOID:2349 arteriosclerosis HGNC:1753 Homo sapiens (human) 1012 CDH13
  • PMID:11326751
DOID:4247 coronary restenosis HGNC:1753 Homo sapiens (human) 1012 CDH13
  • MGI:6194238
DOID:1612 breast cancer HGNC:1753 Homo sapiens (human) 1012 CDH13
  • PMID:17764565
  • PMID:8673923
DOID:10283 prostate cancer HGNC:1753 Homo sapiens (human) 1012 CDH13
  • PMID:18387661
DOID:2871 endometrial carcinoma HGNC:1753 Homo sapiens (human) 1012 CDH13
  • PMID:18519763
DOID:2394 ovarian cancer HGNC:1753 Homo sapiens (human) 1012 CDH13
  • PMID:10493953
DOID:303 substance-related disorder HGNC:1753 Homo sapiens (human) 1012 CDH13
  • MGI:6194238
DOID:3459 breast carcinoma HGNC:1753 Homo sapiens (human) 1012 CDH13
  • PMID:11389090
DOID:3908 lung non-small cell carcinoma HGNC:1753 Homo sapiens (human) 1012 CDH13
  • PMID:11389090

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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