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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 4976 - 5000 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID ▲ Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:0050524 maturity-onset diabetes of the young HGNC:4195 Homo sapiens (human) 2645 GCK
  • MGI:6194238
DOID:4194 glucose metabolism disease HGNC:4195 Homo sapiens (human) 2645 GCK
  • MGI:6194238
DOID:9970 obesity HGNC:4195 Homo sapiens (human) 2645 GCK
  • MGI:6194238
DOID:9993 hypoglycemia HGNC:4195 Homo sapiens (human) 2645 GCK
  • PMID:9435328
DOID:557 kidney disease HGNC:4201 Homo sapiens (human) 2648 KAT2A
  • MGI:6194238
DOID:3908 lung non-small cell carcinoma HGNC:4201 Homo sapiens (human) 2648 KAT2A
  • PMID:23543735
DOID:114 heart disease HGNC:4201 Homo sapiens (human) 2648 KAT2A
  • MGI:6194238
DOID:3211 lysosomal storage disease HGNC:10933 Homo sapiens (human) 26503 SLC17A5
  • MGI:6194238
DOID:3659 sialuria HGNC:10933 Homo sapiens (human) 26503 SLC17A5
  • MGI:6194238
  • PMID:10581036
  • RGD:7240710
DOID:0110242 cataract 13 with adult i phenotype HGNC:4204 Homo sapiens (human) 2651 GCNT2
  • RGD:7240710
DOID:83 cataract HGNC:4204 Homo sapiens (human) 2651 GCNT2
  • PMID:15161861
DOID:0070330 multiple mitochondrial dysfunctions syndrome HGNC:4208 Homo sapiens (human) 2653 GCSH
  • RGD:7240710
DOID:9268 glycine encephalopathy HGNC:4208 Homo sapiens (human) 2653 GCSH
  • MGI:6194238
DOID:9252 amino acid metabolic disorder HGNC:4208 Homo sapiens (human) 2653 GCSH
  • PMID:7070876
DOID:0080572 congenital disorder of glycosylation Iw ZFIN:ZDB-GENE-021015-3 Danio rerio (zebrafish) 266797 stt3a
  • MGI:6194238
DOID:6432 pulmonary hypertension RGD:628656 Rattus norvegicus (Norway rat) 266805 Has3
  • PMID:19915162
DOID:5082 liver cirrhosis WB:WBGene00004049 Caenorhabditis elegans 266823 parp-1
  • MGI:6194238
DOID:2841 asthma WB:WBGene00004049 Caenorhabditis elegans 266823 parp-1
  • MGI:6194238
DOID:6000 congestive heart failure WB:WBGene00004049 Caenorhabditis elegans 266823 parp-1
  • MGI:6194238
DOID:14330 Parkinson's disease WB:WBGene00004049 Caenorhabditis elegans 266823 parp-1
  • MGI:6194238
DOID:848 arthritis WB:WBGene00004049 Caenorhabditis elegans 266823 parp-1
  • MGI:6194238
DOID:9470 bacterial meningitis WB:WBGene00004049 Caenorhabditis elegans 266823 parp-1
  • MGI:6194238
DOID:10652 Alzheimer's disease WB:WBGene00004049 Caenorhabditis elegans 266823 parp-1
  • MGI:6194238
DOID:5199 ureteral obstruction WB:WBGene00004049 Caenorhabditis elegans 266823 parp-1
  • MGI:6194238
DOID:5517 stomach carcinoma WB:WBGene00004049 Caenorhabditis elegans 266823 parp-1
  • 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