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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 2901 - 2925 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID Species ▲ Gene ID Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:11717 neonatal diabetes HGNC:6081 Homo sapiens (human) 3630 INS
  • MGI:6194238
DOID:3500 gallbladder adenocarcinoma HGNC:2707 Homo sapiens (human) 1636 ACE
  • PMID:20438364
DOID:3669 intermittent claudication HGNC:936 Homo sapiens (human) 572 BAD
  • MGI:6194238
DOID:5394 prolactinoma HGNC:9605 Homo sapiens (human) 5743 PTGS2
  • PMID:22580984
DOID:14330 Parkinson's disease HGNC:6876 Homo sapiens (human) 1432 MAPK14
  • MGI:6194238
DOID:10652 Alzheimer's disease HGNC:11007 Homo sapiens (human) 6515 SLC2A3
  • PMID:8179300
DOID:783 end stage renal disease HGNC:6522 Homo sapiens (human) 3931 LCAT
  • MGI:6194238
DOID:9146 visceral leishmaniasis HGNC:11892 Homo sapiens (human) 7124 TNF
  • PMID:12438370
DOID:224 transient cerebral ischemia HGNC:1937 Homo sapiens (human) 1119 CHKA
  • MGI:6194238
DOID:162 cancer HGNC:12009 Homo sapiens (human) 7167 TPI1
  • MGI:6194238
DOID:0080599 Coronavirus infectious disease HGNC:2707 Homo sapiens (human) 1636 ACE
  • PMID:17108019
DOID:9351 diabetes mellitus HGNC:11285 Homo sapiens (human) 6716 SRD5A2
  • MGI:6194238
DOID:1073 renal hypertension HGNC:2622 Homo sapiens (human) 1558 CYP2C8
  • PMID:20495177
DOID:0050588 muscular dystrophy-dystroglycanopathy type B1 HGNC:3622 Homo sapiens (human) 2218 FKTN
  • MGI:6194238
DOID:2986 IgA glomerulonephritis HGNC:10522 Homo sapiens (human) 6296 ACSM3
  • PMID:12484505
DOID:1289 neurodegenerative disease HGNC:13709 Homo sapiens (human) 8560 DEGS1
  • MGI:6194238
DOID:10003 sensorineural hearing loss HGNC:11720 Homo sapiens (human) 7007 TECTA
  • PMID:9590290
  • PMID:9949200
DOID:1712 aortic valve stenosis HGNC:3354 Homo sapiens (human) 2027 ENO3
  • MGI:6194238
DOID:4947 cholangiocarcinoma HGNC:435 Homo sapiens (human) 240 ALOX5
  • PMID:18507031
DOID:1059 intellectual disability HGNC:7680 Homo sapiens (human) 3340 NDST1
  • MGI:6194238
DOID:9256 colorectal cancer HGNC:4553 Homo sapiens (human) 2876 GPX1
  • PMID:19428376
  • PMID:25550558
DOID:0050570 congenital disorder of glycosylation type I HGNC:9114 Homo sapiens (human) 5372 PMM1
  • MGI:6194238
DOID:10908 hydrocephalus HGNC:9232 Homo sapiens (human) 5465 PPARA
  • MGI:6194238
DOID:3908 lung non-small cell carcinoma HGNC:936 Homo sapiens (human) 572 BAD
  • PMID:21918885
  • PMID:24092988
DOID:2256 osteochondrodysplasia HGNC:5273 Homo sapiens (human) 3339 HSPG2
  • PMID:11101850

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Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01


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