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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 10951 - 10975 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID ▲ Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:2256 osteochondrodysplasia RGD:620355 Rattus norvegicus (Norway rat) 84468 Chst3
  • MGI:6194238
DOID:5419 schizophrenia RGD:620355 Rattus norvegicus (Norway rat) 84468 Chst3
  • MGI:6194238
DOID:3343 glycoproteinosis HGNC:23026 Homo sapiens (human) 84572 GNPTG
  • PMID:10712439
DOID:0080678 mucolipidosis III gamma HGNC:23026 Homo sapiens (human) 84572 GNPTG
  • RGD:7240710
DOID:1508 candidiasis RGD:619955 Rattus norvegicus (Norway rat) 84597 Fut9
  • MGI:6194238
DOID:0050861 colorectal adenocarcinoma HGNC:12020 Homo sapiens (human) 8460 TPST1
  • PMID:27354594
DOID:784 chronic kidney disease HGNC:16940 Homo sapiens (human) 84649 DGAT2
  • MGI:6194238
DOID:9452 steatotic liver disease HGNC:16940 Homo sapiens (human) 84649 DGAT2
  • MGI:6194238
DOID:10787 premature menopause HGNC:16940 Homo sapiens (human) 84649 DGAT2
  • MGI:6194238
DOID:0080208 metabolic dysfunction-associated steatotic liver disease HGNC:16940 Homo sapiens (human) 84649 DGAT2
  • MGI:6194238
  • PMID:17618857
DOID:14749 methylmalonic acidemia HGNC:16732 Homo sapiens (human) 84693 MCEE
  • MGI:6194238
DOID:1459 hypothyroidism HGNC:1516 Homo sapiens (human) 847 CAT
  • MGI:6194238
DOID:10825 essential hypertension HGNC:1516 Homo sapiens (human) 847 CAT
  • PMID:15735318
DOID:161 keratosis HGNC:1516 Homo sapiens (human) 847 CAT
  • PMID:14580687
DOID:0060180 colitis HGNC:1516 Homo sapiens (human) 847 CAT
  • MGI:6194238
DOID:13550 angle-closure glaucoma HGNC:1516 Homo sapiens (human) 847 CAT
  • PMID:23961996
DOID:10763 hypertension HGNC:1516 Homo sapiens (human) 847 CAT
  • MGI:6194238
DOID:0081120 Graves ophthalmopathy HGNC:1516 Homo sapiens (human) 847 CAT
  • PMID:15158621
  • PMID:20394549
DOID:1793 pancreatic cancer HGNC:1516 Homo sapiens (human) 847 CAT
  • PMID:12499913
DOID:83 cataract HGNC:1516 Homo sapiens (human) 847 CAT
  • MGI:6194238
  • PMID:15295623
DOID:6000 congestive heart failure HGNC:1516 Homo sapiens (human) 847 CAT
  • PMID:10618301
DOID:10754 otitis media HGNC:1516 Homo sapiens (human) 847 CAT
  • MGI:6194238
DOID:1289 neurodegenerative disease HGNC:1516 Homo sapiens (human) 847 CAT
  • MGI:6194238
DOID:2582 acatalasia HGNC:1516 Homo sapiens (human) 847 CAT
  • RGD:7240710
DOID:10316 pneumoconiosis HGNC:1516 Homo sapiens (human) 847 CAT
  • PMID:19273541

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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: August 19, 2024