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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 2826 - 2850 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID ▲ Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:0080411 familial adenomatous polyposis 3 WB:WBGene00011201 Caenorhabditis elegans 187770 nth-1
  • MGI:6194238
DOID:2615 papilloma MGI:1195256 Mus musculus (house mouse) 18783 Pla2g4a
  • MGI:6194238
DOID:0080322 polycystic kidney disease MGI:1195256 Mus musculus (house mouse) 18783 Pla2g4a
  • MGI:6194238
DOID:2671 transitional cell carcinoma MGI:1195256 Mus musculus (house mouse) 18783 Pla2g4a
  • MGI:6194238
DOID:2841 asthma MGI:1195256 Mus musculus (house mouse) 18783 Pla2g4a
  • MGI:6194238
DOID:4195 hyperglycemia MGI:1195256 Mus musculus (house mouse) 18783 Pla2g4a
  • MGI:6194238
DOID:2316 brain ischemia MGI:1195256 Mus musculus (house mouse) 18783 Pla2g4a
  • MGI:6194238
DOID:1508 candidiasis WB:WBGene00020222 Caenorhabditis elegans 188084 fut-6
  • MGI:6194238
DOID:10763 hypertension WB:WBGene00011517 Caenorhabditis elegans 188169 cgt-1
  • MGI:6194238
DOID:0110296 autosomal recessive limb-girdle muscular dystrophy type 2M WB:WBGene00011554 Caenorhabditis elegans 188207 T07A5.1
  • MGI:6194238
DOID:0110284 autosomal recessive limb-girdle muscular dystrophy type 2L WB:WBGene00011554 Caenorhabditis elegans 188207 T07A5.1
  • MGI:6194238
DOID:9884 muscular dystrophy WB:WBGene00011554 Caenorhabditis elegans 188207 T07A5.1
  • MGI:6194238
DOID:0112379 muscular dystrophy-dystroglycanopathy type B4 WB:WBGene00011554 Caenorhabditis elegans 188207 T07A5.1
  • MGI:6194238
DOID:0110444 dilated cardiomyopathy 1X WB:WBGene00011554 Caenorhabditis elegans 188207 T07A5.1
  • MGI:6194238
DOID:0110443 dilated cardiomyopathy 1B WB:WBGene00011554 Caenorhabditis elegans 188207 T07A5.1
  • MGI:6194238
DOID:0050560 Walker-Warburg syndrome WB:WBGene00011554 Caenorhabditis elegans 188207 T07A5.1
  • MGI:6194238
DOID:0050559 Fukuyama congenital muscular dystrophy WB:WBGene00011554 Caenorhabditis elegans 188207 T07A5.1
  • MGI:6194238
DOID:0050588 muscular dystrophy-dystroglycanopathy type B1 WB:WBGene00011554 Caenorhabditis elegans 188207 T07A5.1
  • MGI:6194238
DOID:0111670 primary hyperoxaluria type 1 HGNC:341 Homo sapiens (human) 189 AGXT
  • MGI:6194238
  • RGD:7240710
DOID:2977 primary hyperoxaluria HGNC:341 Homo sapiens (human) 189 AGXT
  • MGI:6194238
DOID:0080119 mitochondrial DNA depletion syndrome 1 HGNC:3148 Homo sapiens (human) 1890 TYMP
  • RGD:7240710
DOID:4440 seminoma HGNC:3148 Homo sapiens (human) 1890 TYMP
  • PMID:10886088
DOID:4948 gallbladder carcinoma HGNC:3148 Homo sapiens (human) 1890 TYMP
  • PMID:18946757
DOID:3307 teratoma HGNC:3148 Homo sapiens (human) 1890 TYMP
  • PMID:10886088
DOID:3587 pancreatic ductal carcinoma HGNC:3148 Homo sapiens (human) 1890 TYMP
  • PMID:19760965

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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