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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 9101 - 9125 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol ▼ FlyGlycoDB Evidence Code Names References
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:10652 Alzheimer's disease HGNC:24864 Homo sapiens (human) 26330 GAPDHS
  • PMID:15507493
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
DOID:3525 middle cerebral artery infarction HGNC:4141 Homo sapiens (human) 2597 GAPDH
  • MGI:6194238
DOID:0050827 rheumatic heart disease HGNC:4141 Homo sapiens (human) 2597 GAPDH
  • MGI:6194238
DOID:8947 diabetic retinopathy HGNC:4141 Homo sapiens (human) 2597 GAPDH
  • MGI:6194238
DOID:0050866 oral squamous cell carcinoma HGNC:4141 Homo sapiens (human) 2597 GAPDH
  • MGI:6194238
DOID:1826 epilepsy HGNC:4141 Homo sapiens (human) 2597 GAPDH
  • MGI:6194238
DOID:0080322 polycystic kidney disease HGNC:4138 Homo sapiens (human) 23193 GANAB
  • PMID:27259053
DOID:0050770 polycystic liver disease HGNC:4138 Homo sapiens (human) 23193 GANAB
  • PMID:27259053
  • PMID:31462075
DOID:0110860 polycystic kidney disease 3 HGNC:4138 Homo sapiens (human) 23193 GANAB
  • RGD:7240710
DOID:9870 galactosemia HGNC:4135 Homo sapiens (human) 2592 GALT
  • MGI:6194238

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GlyCosmos is a member of the GlySpace Alliance together with GlyGen and Glycomics@ExPASy.

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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