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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 7276 - 7300 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID ▼ Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:9352 type 2 diabetes mellitus RGD:62060 Rattus norvegicus (Norway rat) 26295 Ogt
  • MGI:6194238
DOID:0080240 non-syndromic X-linked intellectual disability 106 RGD:62060 Rattus norvegicus (Norway rat) 26295 Ogt
  • MGI:6194238
DOID:1712 aortic valve stenosis RGD:62060 Rattus norvegicus (Norway rat) 26295 Ogt
  • MGI:6194238
DOID:0050474 Netherton syndrome HGNC:4177 Homo sapiens (human) 2629 GBA1
  • PMID:16601670
DOID:8893 psoriasis HGNC:4177 Homo sapiens (human) 2629 GBA1
  • PMID:15610510
DOID:0112250 Gaucher's disease type IIIC HGNC:4177 Homo sapiens (human) 2629 GBA1
  • RGD:7240710
DOID:0110960 Gaucher's disease perinatal lethal HGNC:4177 Homo sapiens (human) 2629 GBA1
  • RGD:7240710
DOID:0080855 Parkinsonism HGNC:4177 Homo sapiens (human) 2629 GBA1
  • PMID:20838799
DOID:12217 Lewy body dementia HGNC:4177 Homo sapiens (human) 2629 GBA1
  • MGI:6194238
  • PMID:20971030
  • PMID:25933391
  • RGD:7240710
DOID:0060892 late onset Parkinson's disease HGNC:4177 Homo sapiens (human) 2629 GBA1
  • RGD:7240710
DOID:0110957 Gaucher's disease type I HGNC:4177 Homo sapiens (human) 2629 GBA1
  • MGI:6194238
  • RGD:7240710
DOID:0110958 Gaucher's disease type II HGNC:4177 Homo sapiens (human) 2629 GBA1
  • MGI:6194238
  • RGD:7240710
DOID:14330 Parkinson's disease HGNC:4177 Homo sapiens (human) 2629 GBA1
  • MGI:6194238
  • PMID:19945510
  • PMID:20528910
  • PMID:20947659
  • PMID:21242499
  • PMID:24126159
  • PMID:25639775
  • PMID:26223426
DOID:0110959 Gaucher's disease type III HGNC:4177 Homo sapiens (human) 2629 GBA1
  • RGD:7240710
DOID:1926 Gaucher's disease HGNC:4177 Homo sapiens (human) 2629 GBA1
  • MGI:6194238
  • PMID:17059888
  • PMID:18586596
  • PMID:21112800
DOID:0080575 Larsen-like syndrome B3GAT3 type HGNC:923 Homo sapiens (human) 26229 B3GAT3
  • RGD:7240710
DOID:9409 diabetes insipidus ZFIN:ZDB-GENE-020828-1 Danio rerio (zebrafish) 260350 has2
  • MGI:6194238
DOID:6432 pulmonary hypertension ZFIN:ZDB-GENE-020828-1 Danio rerio (zebrafish) 260350 has2
  • MGI:6194238
DOID:3525 middle cerebral artery infarction ZFIN:ZDB-GENE-020828-1 Danio rerio (zebrafish) 260350 has2
  • MGI:6194238
DOID:10763 hypertension HGNC:17855 Homo sapiens (human) 26035 GLCE
  • PMID:27699767
DOID:6713 cerebrovascular disease HGNC:17855 Homo sapiens (human) 26035 GLCE
  • PMID:27699767
DOID:9970 obesity HGNC:4141 Homo sapiens (human) 2597 GAPDH
  • MGI:6194238
DOID:10652 Alzheimer's disease HGNC:4141 Homo sapiens (human) 2597 GAPDH
  • MGI:6194238
  • PMID:15507493
  • PMID:17387692
  • PMID:18340469
  • PMID:20864222
  • PMID:28087189
DOID:0060108 brain glioma HGNC:4141 Homo sapiens (human) 2597 GAPDH
  • MGI:6194238
DOID:3319 lymphangioleiomyomatosis HGNC:4141 Homo sapiens (human) 2597 GAPDH
  • PMID:29885404

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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: August 19, 2024