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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 1326 - 1350 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID ▲ Species Gene ID Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:2986 IgA glomerulonephritis HGNC:10522 Homo sapiens (human) 6296 ACSM3
  • PMID:12484505
DOID:10763 hypertension HGNC:10522 Homo sapiens (human) 6296 ACSM3
  • MGI:6194238
DOID:9282 ocular hypertension HGNC:10522 Homo sapiens (human) 6296 ACSM3
  • MGI:6194238
DOID:8577 ulcerative colitis HGNC:10522 Homo sapiens (human) 6296 ACSM3
  • PMID:21987487
DOID:2581 chondrodysplasia punctata HGNC:10545 Homo sapiens (human) 6307 MSMO1
  • MGI:6194238
DOID:0080547 metabolic dysfunction-associated steatohepatitis HGNC:10571 Homo sapiens (human) 6319 SCD
  • MGI:6194238
DOID:397 restrictive cardiomyopathy HGNC:10571 Homo sapiens (human) 6319 SCD
  • MGI:6194238
DOID:0080208 metabolic dysfunction-associated steatotic liver disease HGNC:10571 Homo sapiens (human) 6319 SCD
  • MGI:6194238
DOID:305 carcinoma HGNC:10571 Homo sapiens (human) 6319 SCD
  • MGI:6194238
DOID:2018 hyperinsulinism HGNC:10571 Homo sapiens (human) 6319 SCD
  • MGI:6194238
DOID:9970 obesity HGNC:10606 Homo sapiens (human) 6342 SCP2
  • MGI:6194238
DOID:905 Zellweger syndrome HGNC:10606 Homo sapiens (human) 6342 SCP2
  • PMID:3555624
DOID:9970 obesity HGNC:10658 Homo sapiens (human) 6382 SDC1
  • MGI:6194238
DOID:4195 hyperglycemia HGNC:10658 Homo sapiens (human) 6382 SDC1
  • PMID:16810465
DOID:1168 familial hyperlipidemia HGNC:10658 Homo sapiens (human) 6382 SDC1
  • MGI:6194238
DOID:8567 Hodgkin's lymphoma HGNC:10658 Homo sapiens (human) 6382 SDC1
  • PMID:9746758
DOID:576 proteinuria HGNC:10658 Homo sapiens (human) 6382 SDC1
  • MGI:6194238
DOID:5844 myocardial infarction HGNC:10658 Homo sapiens (human) 6382 SDC1
  • MGI:6194238
DOID:3910 lung adenocarcinoma HGNC:10658 Homo sapiens (human) 6382 SDC1
  • PMID:23374247
DOID:674 cleft palate HGNC:10659 Homo sapiens (human) 6383 SDC2
  • PMID:18716610
DOID:9352 type 2 diabetes mellitus HGNC:10659 Homo sapiens (human) 6383 SDC2
  • PMID:14976204
DOID:9296 cleft lip HGNC:10659 Homo sapiens (human) 6383 SDC2
  • PMID:18716610
DOID:9970 obesity HGNC:10660 Homo sapiens (human) 9672 SDC3
  • RGD:7240710
DOID:104 bacterial infectious disease HGNC:10661 Homo sapiens (human) 6385 SDC4
  • MGI:6194238
DOID:5844 myocardial infarction HGNC:10661 Homo sapiens (human) 6385 SDC4
  • PMID:11372670

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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