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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 8701 - 8725 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID ▼ Species Gene ID Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:0080208 metabolic dysfunction-associated steatotic liver disease HGNC:288 Homo sapiens (human) 155 ADRB3
  • PMID:15318095
DOID:10763 hypertension HGNC:288 Homo sapiens (human) 155 ADRB3
  • PMID:10981554
DOID:1380 endometrial cancer HGNC:288 Homo sapiens (human) 155 ADRB3
  • PMID:15743038
DOID:11612 polycystic ovary syndrome HGNC:288 Homo sapiens (human) 155 ADRB3
  • MGI:6194238
DOID:0060180 colitis HGNC:288 Homo sapiens (human) 155 ADRB3
  • MGI:6194238
DOID:1485 cystic fibrosis HGNC:288 Homo sapiens (human) 155 ADRB3
  • PMID:20203292
DOID:9352 type 2 diabetes mellitus HGNC:288 Homo sapiens (human) 155 ADRB3
  • PMID:16444766
  • PMID:17727676
  • PMID:19659999
DOID:6000 congestive heart failure HGNC:288 Homo sapiens (human) 155 ADRB3
  • MGI:6194238
  • PMID:11273992
DOID:3393 coronary artery disease HGNC:288 Homo sapiens (human) 155 ADRB3
  • PMID:11229427
  • PMID:9126344
DOID:10783 methemoglobinemia HGNC:2873 Homo sapiens (human) 1727 CYB5R3
  • PMID:11295830
DOID:1612 breast cancer HGNC:2873 Homo sapiens (human) 1727 CYB5R3
  • PMID:25225034
DOID:0060076 estrogen-receptor negative breast cancer HGNC:2873 Homo sapiens (human) 1727 CYB5R3
  • PMID:26351264
DOID:14692 Smith-Lemli-Opitz syndrome HGNC:2860 Homo sapiens (human) 1717 DHCR7
  • MGI:6194238
  • PMID:9683613
  • RGD:7240710
DOID:13241 Behcet's disease HGNC:2860 Homo sapiens (human) 1717 DHCR7
  • PMID:24184224
DOID:0111230 congenital muscular dystrophy-dystroglycanopathy type A11 HGNC:28596 Homo sapiens (human) 148789 B3GALNT2
  • RGD:7240710
DOID:3146 lipid metabolism disorder HGNC:2859 Homo sapiens (human) 1718 DHCR24
  • PMID:11519011
DOID:4194 glucose metabolism disease HGNC:2853 Homo sapiens (human) 1608 DGKG
  • MGI:6194238
DOID:0060227 Adams-Oliver syndrome HGNC:28526 Homo sapiens (human) 285203 EOGT
  • RGD:7240710
DOID:0080388 nephrotic syndrome type 7 HGNC:2852 Homo sapiens (human) 8526 DGKE
  • RGD:7240710
DOID:0050561 Lennox-Gastaut syndrome HGNC:2851 Homo sapiens (human) 8527 DGKD
  • MGI:6194238
DOID:4194 glucose metabolism disease HGNC:2850 Homo sapiens (human) 1607 DGKB
  • MGI:6194238
DOID:4194 glucose metabolism disease HGNC:2849 Homo sapiens (human) 1606 DGKA
  • MGI:6194238
DOID:784 chronic kidney disease HGNC:2843 Homo sapiens (human) 8694 DGAT1
  • MGI:6194238
DOID:1184 nephrotic syndrome HGNC:2843 Homo sapiens (human) 8694 DGAT1
  • MGI:6194238
DOID:0050700 cardiomyopathy HGNC:2843 Homo sapiens (human) 8694 DGAT1
  • PMID:21220706

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GlyCosmos is a member of the GlySpace Alliance together with GlyGen and Glycomics@ExPASy.

Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

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


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