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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 2101 - 2125 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB ▲ Evidence Code Names References
DOID:12217 Lewy body dementia HGNC:4177 Homo sapiens (human) 2629 GBA1
  • MGI:6194238
  • PMID:20971030
  • PMID:25933391
  • RGD:7240710
DOID:9352 type 2 diabetes mellitus MGI:107474 Mus musculus (house mouse) 12494 Cd38
  • MGI:6194238
DOID:5212 congenital disorder of glycosylation WB:WBGene00010720 Caenorhabditis elegans 175065 algn-3
  • MGI:6194238
DOID:2741 bilirubin metabolic disorder FB:FBgn0040255 Drosophila melanogaster (fruit fly) 53506 Ugt35E2
  • MGI:6194238
DOID:9256 colorectal cancer RGD:2082 Rattus norvegicus (Norway rat) 25233 Akt2
  • MGI:6194238
  • PMID:11756242
DOID:0060900 Parkinson's disease 14 HGNC:9039 Homo sapiens (human) 8398 PLA2G6
  • MGI:6194238
  • RGD:7240710
DOID:0060480 left ventricular noncompaction HGNC:20862 Homo sapiens (human) 64116 SLC39A8
  • MGI:6194238
DOID:14654 prostatitis HGNC:2594 Homo sapiens (human) 1588 CYP19A1
  • PMID:19700748
DOID:2841 asthma WB:WBGene00004049 Caenorhabditis elegans 266823 parp-1
  • MGI:6194238
DOID:0112321 alacrima, achalasia, and impaired intellectual development syndrome HGNC:22923 Homo sapiens (human) 29926 GMPPA
  • MGI:6194238
  • RGD:7240710
DOID:0080576 spondyloepimetaphyseal dysplasia, Genevieve-type HGNC:19237 Homo sapiens (human) 54187 NANS
  • RGD:7240710
DOID:0080575 Larsen-like syndrome B3GAT3 type HGNC:923 Homo sapiens (human) 26229 B3GAT3
  • RGD:7240710
DOID:893 Wilson disease MGI:98325 Mus musculus (house mouse) 20597 Smpd1
  • MGI:6194238
DOID:2043 hepatitis B MGI:98898 Mus musculus (house mouse) 394436 Ugt1a1
  • MGI:6194238
DOID:3181 oligodendroglioma RGD:1561913 Rattus norvegicus (Norway rat) 362809 Ptges3
  • MGI:6194238
DOID:684 hepatocellular carcinoma HGNC:4056 Homo sapiens (human) 2538 G6PC1
  • PMID:28096054
DOID:8947 diabetic retinopathy WB:WBGene00001686 Caenorhabditis elegans 174578 gpd-4
  • MGI:6194238
DOID:4928 intrahepatic cholangiocarcinoma RGD:1597139 Rattus norvegicus (Norway rat) 361596 Idh2
  • MGI:6194238
DOID:684 hepatocellular carcinoma MGI:1206581 Mus musculus (house mouse) 18706 Pik3ca
  • MGI:6194238
DOID:0050535 exudative vitreoretinopathy MGI:1278315 Mus musculus (house mouse) 16973 Lrp5
  • PMID:18263894
  • PMID:27524797
  • PMID:33497368
DOID:4450 renal cell carcinoma RGD:1305756 Rattus norvegicus (Norway rat) 315219 Tymp
  • MGI:6194238
DOID:8577 ulcerative colitis MGI:96434 Mus musculus (house mouse) 16002 Igf2
  • MGI:6194238
DOID:10283 prostate cancer HGNC:9156 Homo sapiens (human) 5407 PNLIPRP1
  • PMID:11384102
DOID:3393 coronary artery disease RGD:3870 Rattus norvegicus (Norway rat) 29260 Tlr4
  • MGI:6194238
DOID:7998 hyperthyroidism SGD:S000005284 Saccharomyces cerevisiae S288C 855732 CIT1
  • MGI:6194238

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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