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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 10976 - 11000 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB ▲ Evidence Code Names References
DOID:0080208 metabolic dysfunction-associated steatotic liver disease MGI:104993 Mus musculus (house mouse) 16847 Lepr
  • MGI:6194238
  • PMID:22118645
DOID:2978 carbohydrate metabolic disorder SGD:S000002457 Saccharomyces cerevisiae S288C 851620 TPI1
  • MGI:6194238
DOID:2841 asthma HGNC:1932 Homo sapiens (human) 1116 CHI3L1
  • PMID:18003958
  • PMID:19414556
  • PMID:19568425
  • RGD:7240710
DOID:3803 Crigler-Najjar syndrome Xenbase:XB-GENE-5793241 Xenopus tropicalis (tropical clawed frog) 100135191 ugt1a6
  • MGI:6194238
DOID:3525 middle cerebral artery infarction MGI:104798 Mus musculus (house mouse) 21926 Tnf
  • MGI:6194238
DOID:9538 multiple myeloma WB:WBGene00000503 Caenorhabditis elegans 180628 cht-1
  • MGI:6194238
DOID:0081120 Graves ophthalmopathy MGI:104798 Mus musculus (house mouse) 21926 Tnf
  • MGI:6194238
DOID:1612 breast cancer HGNC:936 Homo sapiens (human) 572 BAD
  • PMID:17004114
DOID:2394 ovarian cancer RGD:620874 Rattus norvegicus (Norway rat) 89824 Chi3l1
  • MGI:6194238
DOID:9970 obesity HGNC:385 Homo sapiens (human) 1646 AKR1C2
  • PMID:15494612
DOID:5016 hepatocellular clear cell carcinoma RGD:3001 Rattus norvegicus (Norway rat) 24536 Lepr
  • MGI:6194238
DOID:77 gastrointestinal system disease HGNC:5466 Homo sapiens (human) 3481 IGF2
  • PMID:16477536
DOID:0080564 congenital disorder of glycosylation Il RGD:1311272 Rattus norvegicus (Norway rat) 367083 Alg9
  • MGI:6194238
DOID:0050830 peripheral artery disease HGNC:13633 Homo sapiens (human) 9370 ADIPOQ
  • PMID:16321391
DOID:9206 Barrett's esophagus Xenbase:XB-GENE-921709 Xenopus laevis (African clawed frog) 733177 b3gat2.S
  • MGI:6194238
DOID:1289 neurodegenerative disease HGNC:9039 Homo sapiens (human) 8398 PLA2G6
  • MGI:6194238
DOID:0060307 autosomal dominant intellectual developmental disorder HGNC:19263 Homo sapiens (human) 81562 LMAN2L
  • RGD:7240710
DOID:0111933 phosphoglycerate kinase 1 deficiency WB:WBGene00020185 Caenorhabditis elegans 171965 pgk-1
  • MGI:6194238
DOID:3083 chronic obstructive pulmonary disease RGD:2059 Rattus norvegicus (Norway rat) 24925 Adrb1
  • MGI:6194238
DOID:10591 pre-eclampsia MGI:88470 Mus musculus (house mouse) 12846 Comt
  • PMID:18469803
DOID:1682 congenital heart disease HGNC:4555 Homo sapiens (human) 2878 GPX3
  • PMID:26612412
DOID:0060071 pre-malignant neoplasm HGNC:11998 Homo sapiens (human) 7157 TP53
  • MGI:6194238
DOID:5082 liver cirrhosis MGI:96434 Mus musculus (house mouse) 16002 Igf2
  • MGI:6194238
DOID:6713 cerebrovascular disease WB:WBGene00007108 Caenorhabditis elegans 178046 gspd-1
  • MGI:6194238
DOID:11168 anogenital venereal wart MGI:96824 Mus musculus (house mouse) 21898 Tlr4
  • MGI:6194238

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

Acknowledgements

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