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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 10851 - 10875 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 WB:WBGene00008706 Caenorhabditis elegans 178535 gba-3
  • MGI:6194238
DOID:1926 Gaucher's disease WB:WBGene00008706 Caenorhabditis elegans 178535 gba-3
  • MGI:6194238
DOID:0080855 Parkinsonism WB:WBGene00008706 Caenorhabditis elegans 178535 gba-3
  • MGI:6194238
DOID:0112250 Gaucher's disease type IIIC WB:WBGene00008706 Caenorhabditis elegans 178535 gba-3
  • MGI:6194238
DOID:0110957 Gaucher's disease type I WB:WBGene00008706 Caenorhabditis elegans 178535 gba-3
  • MGI:6194238
DOID:0050474 Netherton syndrome WB:WBGene00008706 Caenorhabditis elegans 178535 gba-3
  • MGI:6194238
DOID:0110959 Gaucher's disease type III WB:WBGene00008706 Caenorhabditis elegans 178535 gba-3
  • MGI:6194238
DOID:14330 Parkinson's disease WB:WBGene00008706 Caenorhabditis elegans 178535 gba-3
  • MGI:6194238
DOID:0110960 Gaucher's disease perinatal lethal WB:WBGene00008706 Caenorhabditis elegans 178535 gba-3
  • MGI:6194238
DOID:0110958 Gaucher's disease type II WB:WBGene00008706 Caenorhabditis elegans 178535 gba-3
  • MGI:6194238
DOID:12217 Lewy body dementia WB:WBGene00008706 Caenorhabditis elegans 178535 gba-3
  • MGI:6194238
DOID:0070254 congenital disorder of glycosylation type IIb WB:WBGene00008775 Caenorhabditis elegans 177998 mogs-1
  • MGI:6194238
DOID:0050570 congenital disorder of glycosylation type I WB:WBGene00009925 Caenorhabditis elegans 178364 F52B11.2
  • MGI:6194238
DOID:5212 congenital disorder of glycosylation WB:WBGene00009925 Caenorhabditis elegans 178364 F52B11.2
  • MGI:6194238
DOID:0080552 congenital disorder of glycosylation Ia WB:WBGene00009925 Caenorhabditis elegans 178364 F52B11.2
  • MGI:6194238
DOID:0060227 Adams-Oliver syndrome WB:WBGene00010386 Caenorhabditis elegans 179990 H12D21.10
  • MGI:6194238
DOID:0050588 muscular dystrophy-dystroglycanopathy type B1 WB:WBGene00010694 Caenorhabditis elegans 3565692 bgnt-1.5
  • MGI:6194238
DOID:0111238 congenital muscular dystrophy-dystroglycanopathy type A13 WB:WBGene00010694 Caenorhabditis elegans 3565692 bgnt-1.5
  • MGI:6194238
DOID:0111242 congenital muscular dystrophy-dystroglycanopathy type A6 WB:WBGene00010716 Caenorhabditis elegans 187206 lge-1
  • MGI:6194238
DOID:0050588 muscular dystrophy-dystroglycanopathy type B1 WB:WBGene00010716 Caenorhabditis elegans 187206 lge-1
  • MGI:6194238
DOID:0110637 muscular dystrophy-dystroglycanopathy type B6 WB:WBGene00010716 Caenorhabditis elegans 187206 lge-1
  • MGI:6194238
DOID:11727 facioscapulohumeral muscular dystrophy WB:WBGene00010716 Caenorhabditis elegans 187206 lge-1
  • MGI:6194238
DOID:5212 congenital disorder of glycosylation WB:WBGene00010720 Caenorhabditis elegans 175065 algn-3
  • MGI:6194238
DOID:0080556 congenital disorder of glycosylation Id WB:WBGene00010720 Caenorhabditis elegans 175065 algn-3
  • MGI:6194238
DOID:14250 Down syndrome WB:WBGene00010757 Caenorhabditis elegans 259529 pad-2
  • PMID:15233996

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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