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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 5051 - 5075 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol ▲ FlyGlycoDB Evidence Code Names References
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:557 kidney disease HGNC:15527 Homo sapiens (human) 152831 KLB
  • MGI:6194238
DOID:1883 hepatitis C HGNC:6374 Homo sapiens (human) 3821 KLRC1
  • PMID:17553896
DOID:1883 hepatitis C HGNC:18788 Homo sapiens (human) 22914 KLRK1
  • PMID:26518141
  • PMID:27091211
DOID:4231 histiocytoma HGNC:18788 Homo sapiens (human) 22914 KLRK1
  • MGI:6194238
DOID:11168 anogenital venereal wart HGNC:18788 Homo sapiens (human) 22914 KLRK1
  • PMID:23754510
DOID:0060704 lymphoproliferative syndrome HGNC:18788 Homo sapiens (human) 22914 KLRK1
  • PMID:22105417
DOID:399 tuberculosis HGNC:18788 Homo sapiens (human) 22914 KLRK1
  • PMID:23922903
DOID:321 tropical spastic paraparesis HGNC:18788 Homo sapiens (human) 22914 KLRK1
  • PMID:22170554
DOID:114 heart disease MGI:1343101 Mus musculus (house mouse) 14534 Kat2a
  • MGI:6194238
DOID:557 kidney disease MGI:1343101 Mus musculus (house mouse) 14534 Kat2a
  • MGI:6194238
DOID:3908 lung non-small cell carcinoma MGI:1343101 Mus musculus (house mouse) 14534 Kat2a
  • MGI:6194238

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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