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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 7151 - 7175 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol ▼ FlyGlycoDB Evidence Code Names References
DOID:1883 hepatitis C HGNC:6374 Homo sapiens (human) 3821 KLRC1
  • PMID:17553896
DOID:557 kidney disease HGNC:15527 Homo sapiens (human) 152831 KLB
  • MGI:6194238
DOID:2247 spondylosis HGNC:6344 Homo sapiens (human) 9365 KL
  • PMID:12110410
DOID:10763 hypertension HGNC:6344 Homo sapiens (human) 9365 KL
  • MGI:6194238
DOID:12466 secondary hyperparathyroidism HGNC:6344 Homo sapiens (human) 9365 KL
  • MGI:6194238
DOID:9352 type 2 diabetes mellitus HGNC:6344 Homo sapiens (human) 9365 KL
  • MGI:6194238
DOID:557 kidney disease HGNC:6344 Homo sapiens (human) 9365 KL
  • MGI:6194238
DOID:4372 intracranial embolism HGNC:6344 Homo sapiens (human) 9365 KL
  • PMID:16973281
DOID:0111063 hyperphosphatemic familial tumoral calcinosis HGNC:6344 Homo sapiens (human) 9365 KL
  • MGI:6194238
DOID:784 chronic kidney disease HGNC:6344 Homo sapiens (human) 9365 KL
  • MGI:6194238
  • PMID:21115613
DOID:783 end stage renal disease HGNC:6344 Homo sapiens (human) 9365 KL
  • MGI:6194238
  • PMID:11162628
DOID:1168 familial hyperlipidemia HGNC:6344 Homo sapiens (human) 9365 KL
  • MGI:6194238
DOID:9675 pulmonary emphysema HGNC:6344 Homo sapiens (human) 9365 KL
  • MGI:6194238
DOID:10584 retinitis pigmentosa HGNC:6344 Homo sapiens (human) 9365 KL
  • MGI:6194238
DOID:3393 coronary artery disease HGNC:6344 Homo sapiens (human) 9365 KL
  • PMID:16579981
  • PMID:16979405
DOID:1074 kidney failure HGNC:6344 Homo sapiens (human) 9365 KL
  • MGI:6194238
DOID:0111680 essential fructosuria HGNC:6315 Homo sapiens (human) 3795 KHK
  • RGD:7240710
DOID:0050873 follicular lymphoma HGNC:4021 Homo sapiens (human) 2531 KDSR
  • PMID:8417785
DOID:0080250 erythrokeratodermia variabilis et progressiva 4 HGNC:4021 Homo sapiens (human) 2531 KDSR
  • MGI:6194238
  • RGD:7240710
DOID:409 liver disease HGNC:4021 Homo sapiens (human) 2531 KDSR
  • MGI:6194238
DOID:1588 thrombocytopenia HGNC:4021 Homo sapiens (human) 2531 KDSR
  • MGI:6194238
DOID:0060224 atrial fibrillation HGNC:6294 Homo sapiens (human) 3784 KCNQ1
  • PMID:12522251
DOID:2842 Jervell-Lange Nielsen syndrome HGNC:6294 Homo sapiens (human) 3784 KCNQ1
  • MGI:6194238
  • PMID:12051962
  • RGD:7240710
DOID:2843 long QT syndrome HGNC:6294 Homo sapiens (human) 3784 KCNQ1
  • MGI:6194238
  • PMID:15840476
  • PMID:22199116
DOID:9352 type 2 diabetes mellitus HGNC:6294 Homo sapiens (human) 3784 KCNQ1
  • PMID:27281273

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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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Last updated: August 19, 2024