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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 6951 - 6975 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID Species ▼ Gene ID Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:3526 cerebral infarction HGNC:3402 Homo sapiens (human) 2053 EPHX2
  • MGI:6194238
DOID:10283 prostate cancer HGNC:392 Homo sapiens (human) 208 AKT2
  • PMID:22815832
DOID:10247 pleurisy HGNC:435 Homo sapiens (human) 240 ALOX5
  • MGI:6194238
DOID:0050571 congenital disorder of glycosylation type II HGNC:30760 Homo sapiens (human) 55858 TMEM165
  • MGI:6194238
DOID:0060074 ductal carcinoma in situ HGNC:11755 Homo sapiens (human) 7031 TFF1
  • PMID:15375487
DOID:10247 pleurisy HGNC:9605 Homo sapiens (human) 5743 PTGS2
  • MGI:6194238
DOID:12351 alcoholic hepatitis HGNC:2328 Homo sapiens (human) 1374 CPT1A
  • MGI:6194238
DOID:0050866 oral squamous cell carcinoma HGNC:9588 Homo sapiens (human) 5728 PTEN
  • PMID:33109573
DOID:4676 uremia HGNC:2228 Homo sapiens (human) 1312 COMT
  • PMID:7437264
DOID:0080322 polycystic kidney disease HGNC:9604 Homo sapiens (human) 5742 PTGS1
  • MGI:6194238
DOID:1289 neurodegenerative disease HGNC:24768 Homo sapiens (human) 375775 PNPLA7
  • MGI:6194238
DOID:13001 carotid stenosis HGNC:9603 Homo sapiens (human) 5740 PTGIS
  • PMID:28704403
DOID:3068 glioblastoma HGNC:9604 Homo sapiens (human) 5742 PTGS1
  • MGI:6194238
  • PMID:11121536
DOID:10763 hypertension HGNC:2590 Homo sapiens (human) 1583 CYP11A1
  • MGI:6194238
DOID:9256 colorectal cancer HGNC:8975 Homo sapiens (human) 5290 PIK3CA
  • RGD:7240710
DOID:4989 pancreatitis HGNC:12663 Homo sapiens (human) 7412 VCAM1
  • PMID:12923961
DOID:0111822 CHILD syndrome HGNC:13398 Homo sapiens (human) 50814 NSDHL
  • RGD:7240710
DOID:0110352 retinitis pigmentosa 59 HGNC:20603 Homo sapiens (human) 79947 DHDDS
  • MGI:6194238
  • RGD:7240710
DOID:1205 allergic disease HGNC:381 Homo sapiens (human) 231 AKR1B1
  • MGI:6194238
DOID:869 cholesteatoma HGNC:11848 Homo sapiens (human) 7097 TLR2
  • PMID:22883581
DOID:3083 chronic obstructive pulmonary disease HGNC:9053 Homo sapiens (human) 5329 PLAUR
  • MGI:6194238
DOID:12377 spinal muscular atrophy HGNC:4879 Homo sapiens (human) 3074 HEXB
  • PMID:1720305
DOID:1059 intellectual disability HGNC:6126 Homo sapiens (human) 8660 IRS2
  • MGI:6194238
DOID:10964 cholesteatoma of middle ear HGNC:11892 Homo sapiens (human) 7124 TNF
  • PMID:21311206
DOID:9206 Barrett's esophagus HGNC:4559 Homo sapiens (human) 2882 GPX7
  • PMID:18664505

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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