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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 4401 - 4425 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID Species ▲ Gene ID Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:10652 Alzheimer's disease HGNC:3350 Homo sapiens (human) 2023 ENO1
  • PMID:17387692
DOID:12801 mucopolysaccharidosis III HGNC:10818 Homo sapiens (human) 6448 SGSH
  • MGI:6194238
  • PMID:15902564
DOID:783 end stage renal disease HGNC:2328 Homo sapiens (human) 1374 CPT1A
  • MGI:6194238
DOID:9970 obesity HGNC:4241 Homo sapiens (human) 2673 GFPT1
  • PMID:11118009
DOID:12798 mucopolysaccharidosis HGNC:25239 Homo sapiens (human) 153642 ARSK
  • MGI:6194238
  • RGD:7240710
DOID:0060041 autism spectrum disorder HGNC:10982 Homo sapiens (human) 8604 SLC25A12
  • PMID:17151801
  • PMID:18180767
DOID:1826 epilepsy HGNC:108 Homo sapiens (human) 43 ACHE
  • PMID:7634486
DOID:9352 type 2 diabetes mellitus HGNC:1848 Homo sapiens (human) 1056 CEL
  • PMID:16369531
DOID:9970 obesity HGNC:21298 Homo sapiens (human) 65985 AACS
  • MGI:6194238
DOID:10652 Alzheimer's disease HGNC:9237 Homo sapiens (human) 10891 PPARGC1A
  • MGI:6194238
  • PMID:19273754
DOID:5419 schizophrenia HGNC:7656 Homo sapiens (human) 4684 NCAM1
  • PMID:30664618
DOID:893 Wilson disease HGNC:543 Homo sapiens (human) 308 ANXA5
  • MGI:6194238
DOID:3121 gallbladder cancer HGNC:2593 Homo sapiens (human) 1586 CYP17A1
  • PMID:16381022
DOID:0080208 metabolic dysfunction-associated steatotic liver disease HGNC:14934 Homo sapiens (human) 51548 SIRT6
  • MGI:6194238
DOID:2841 asthma HGNC:9035 Homo sapiens (human) 5321 PLA2G4A
  • MGI:6194238
DOID:162 cancer HGNC:8997 Homo sapiens (human) 5305 PIP4K2A
  • MGI:6194238
DOID:1574 alcohol use disorder HGNC:404 Homo sapiens (human) 217 ALDH2
  • PMID:10780266
DOID:0060041 autism spectrum disorder HGNC:20779 Homo sapiens (human) 64579 NDST4
  • MGI:6194238
DOID:1115 sarcoma HGNC:21350 Homo sapiens (human) 8050 PDHX
  • PMID:31089155
DOID:8725 vascular dementia HGNC:4617 Homo sapiens (human) 2932 GSK3B
  • MGI:6194238
DOID:3393 coronary artery disease HGNC:5208 Homo sapiens (human) 3290 HSD11B1
  • PMID:23009206
DOID:1067 open-angle glaucoma HGNC:4369 Homo sapiens (human) 2762 GMDS
  • PMID:25173105
DOID:3454 brain infarction HGNC:8605 Homo sapiens (human) 8505 PARG
  • MGI:6194238
DOID:0110861 autosomal recessive polycystic kidney disease HGNC:391 Homo sapiens (human) 207 AKT1
  • MGI:6194238
DOID:9744 type 1 diabetes mellitus HGNC:11850 Homo sapiens (human) 7099 TLR4
  • PMID:18029454

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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