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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 October 9, 2024
Displaying entries 68701 - 68725 of 71927 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB Evidence Code Names References ▲
DOID:12704 ataxia telangiectasia HGNC:6001 Homo sapiens (human) 3558 IL2
  • PMID:6432389
DOID:12704 ataxia telangiectasia HGNC:5438 Homo sapiens (human) 3458 IFNG
  • PMID:6432389
DOID:9182 pemphigus HGNC:6001 Homo sapiens (human) 3558 IL2
  • PMID:6432916
DOID:11758 iron deficiency anemia HGNC:5141 Homo sapiens (human) 3240 HP
  • PMID:647925
DOID:8893 psoriasis HGNC:1248 Homo sapiens (human) 717 C2
  • PMID:6559061
DOID:10763 hypertension RGD:2445 Rattus norvegicus (Norway rat) 25423 Ctsc
  • PMID:657443
DOID:9119 acute myeloid leukemia HGNC:4458 Homo sapiens (human) 2821 GPI
  • PMID:6589021
DOID:9952 acute lymphoblastic leukemia HGNC:4458 Homo sapiens (human) 2821 GPI
  • PMID:6589021
DOID:2349 arteriosclerosis HGNC:616 Homo sapiens (human) 350 APOH
  • PMID:6613192
DOID:783 end stage renal disease HGNC:3778 Homo sapiens (human) 2335 FN1
  • PMID:6665521
DOID:8924 autoimmune thrombocytopenic purpura HGNC:399 Homo sapiens (human) 213 ALB
  • PMID:6683982
DOID:234 colon adenocarcinoma HGNC:8863 Homo sapiens (human) 5198 PFAS
  • PMID:6722784
DOID:4450 renal cell carcinoma HGNC:8863 Homo sapiens (human) 5198 PFAS
  • PMID:6722784
DOID:1837 diabetic ketoacidosis HGNC:11583 Homo sapiens (human) 6906 SERPINA7
  • PMID:6768790
DOID:11714 gestational diabetes HGNC:612 Homo sapiens (human) 347 APOD
  • PMID:6828336
DOID:14018 alcoholic liver cirrhosis HGNC:11764 Homo sapiens (human) 7038 TG
  • PMID:6883738
DOID:8893 psoriasis HGNC:3327 Homo sapiens (human) 2006 ELN
  • PMID:6893335
DOID:3308 embryonal carcinoma HGNC:317 Homo sapiens (human) 174 AFP
  • PMID:68943
DOID:3305 teratocarcinoma HGNC:317 Homo sapiens (human) 174 AFP
  • PMID:68943
DOID:13241 Behcet's disease HGNC:1037 Homo sapiens (human) 629 CFB
  • PMID:6900632
DOID:12134 factor VIII deficiency HGNC:8864 Homo sapiens (human) 5199 CFP
  • PMID:6912882
DOID:12134 factor VIII deficiency HGNC:1037 Homo sapiens (human) 629 CFB
  • PMID:6912882
DOID:12134 factor VIII deficiency HGNC:1331 Homo sapiens (human) 727 C5
  • PMID:6912882
DOID:12134 factor VIII deficiency HGNC:1318 Homo sapiens (human) 718 C3
  • PMID:6912882
DOID:12241 beta thalassemia HGNC:1037 Homo sapiens (human) 629 CFB
  • PMID:6914868

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

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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: December 9, 2024