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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 69151 - 69175 of 71927 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB Evidence Code Names References ▲
DOID:1459 hypothyroidism RGD:621351 Rattus norvegicus (Norway rat) 84352 Col1a2
  • PMID:8745212
DOID:10652 Alzheimer's disease HGNC:3192 Homo sapiens (human) 1917 EEF1A2
  • PMID:8750861
DOID:11984 hypertrophic cardiomyopathy HGNC:2097 Homo sapiens (human) 1215 CMA1
  • PMID:8759823
DOID:10763 hypertension RGD:3177 Rattus norvegicus (Norway rat) 24596 Ngfr
  • PMID:8762194
DOID:12918 thromboangiitis obliterans HGNC:3327 Homo sapiens (human) 2006 ELN
  • PMID:8763587
DOID:4608 common bile duct neoplasm HGNC:7508 Homo sapiens (human) 4582 MUC1
  • PMID:8766528
DOID:11204 allergic conjunctivitis HGNC:5344 Homo sapiens (human) 3383 ICAM1
  • PMID:8766745
DOID:10952 nephritis RGD:2857 Rattus norvegicus (Norway rat) 25464 Icam1
  • PMID:8773354
DOID:0050663 Bethlem myopathy HGNC:2212 Homo sapiens (human) 1292 COL6A2
  • PMID:8782832
  • RGD:7240710
DOID:0050700 cardiomyopathy HGNC:12373 Homo sapiens (human) 7253 TSHR
  • PMID:8796147
DOID:552 pneumonia RGD:2890 Rattus norvegicus (Norway rat) 24493 Il1a
  • PMID:8806881
DOID:3008 invasive ductal carcinoma HGNC:7739 Homo sapiens (human) 4747 NEFL
  • PMID:8814452
DOID:4440 seminoma HGNC:6407 Homo sapiens (human) 3845 KRAS
  • PMID:8816895
DOID:10652 Alzheimer's disease HGNC:6180 Homo sapiens (human) 3708 ITPR1
  • PMID:8819138
DOID:1682 congenital heart disease MGI:98214 Mus musculus (house mouse) 20181 Rxra
  • PMID:8823298
DOID:3312 bipolar disorder HGNC:5295 Homo sapiens (human) 3358 HTR2C
  • PMID:8823764
DOID:2018 hyperinsulinism RGD:67383 Rattus norvegicus (Norway rat) 170538 Prkcd
  • PMID:8826977
DOID:10487 Hirschsprung's disease HGNC:6342 Homo sapiens (human) 3815 KIT
  • PMID:8831584
  • PMID:9247236
DOID:591 phobic disorder HGNC:5173 Homo sapiens (human) 3265 HRAS
  • PMID:8832771
DOID:10933 obsessive-compulsive disorder HGNC:5173 Homo sapiens (human) 3265 HRAS
  • PMID:8832771
DOID:1574 alcohol use disorder RGD:3213 Rattus norvegicus (Norway rat) 25054 Ntrk2
  • PMID:8840027
DOID:0080322 polycystic kidney disease RGD:2447 Rattus norvegicus (Norway rat) 25425 Ctsh
  • PMID:8840269
DOID:2921 glomerulonephritis HGNC:1241 Homo sapiens (human) 712 C1QA
  • PMID:8840296
DOID:0110106 atrial heart septal defect 1 MGI:97380 Mus musculus (house mouse) 18205 Ntf3
  • PMID:8841198
DOID:6419 tetralogy of Fallot MGI:97380 Mus musculus (house mouse) 18205 Ntf3
  • PMID:8841198

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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