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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 5101 - 5125 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID ▲ Species Gene ID Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:423 myopathy HGNC:7448 Homo sapiens (human) 4534 MTM1
  • MGI:6194238
DOID:14717 centronuclear myopathy HGNC:7448 Homo sapiens (human) 4534 MTM1
  • MGI:6194238
DOID:0111225 centronuclear myopathy X-linked HGNC:7449 Homo sapiens (human) 8776 MTMR1
  • MGI:6194238
DOID:10595 Charcot-Marie-Tooth disease HGNC:7449 Homo sapiens (human) 8776 MTMR1
  • MGI:6194238
DOID:423 myopathy HGNC:7449 Homo sapiens (human) 8776 MTMR1
  • MGI:6194238
DOID:10595 Charcot-Marie-Tooth disease HGNC:7450 Homo sapiens (human) 8898 MTMR2
  • MGI:6194238
DOID:0110191 Charcot-Marie-Tooth disease type 4B1 HGNC:7450 Homo sapiens (human) 8898 MTMR2
  • MGI:6194238
  • RGD:7240710
DOID:0111225 centronuclear myopathy X-linked HGNC:7450 Homo sapiens (human) 8898 MTMR2
  • MGI:6194238
DOID:423 myopathy HGNC:7450 Homo sapiens (human) 8898 MTMR2
  • MGI:6194238
DOID:0111225 centronuclear myopathy X-linked HGNC:7451 Homo sapiens (human) 8897 MTMR3
  • MGI:6194238
DOID:10595 Charcot-Marie-Tooth disease HGNC:7451 Homo sapiens (human) 8897 MTMR3
  • MGI:6194238
DOID:0111225 centronuclear myopathy X-linked HGNC:7452 Homo sapiens (human) 9110 MTMR4
  • MGI:6194238
DOID:10595 Charcot-Marie-Tooth disease HGNC:7452 Homo sapiens (human) 9110 MTMR4
  • MGI:6194238
DOID:767 muscular atrophy HGNC:7452 Homo sapiens (human) 9110 MTMR4
  • MGI:6194238
DOID:10595 Charcot-Marie-Tooth disease HGNC:7453 Homo sapiens (human) 9107 MTMR6
  • MGI:6194238
DOID:14717 centronuclear myopathy HGNC:7453 Homo sapiens (human) 9107 MTMR6
  • MGI:6194238
DOID:0111225 centronuclear myopathy X-linked HGNC:7453 Homo sapiens (human) 9107 MTMR6
  • MGI:6194238
DOID:0111225 centronuclear myopathy X-linked HGNC:7454 Homo sapiens (human) 9108 MTMR7
  • MGI:6194238
DOID:10595 Charcot-Marie-Tooth disease HGNC:7454 Homo sapiens (human) 9108 MTMR7
  • MGI:6194238
DOID:14717 centronuclear myopathy HGNC:7454 Homo sapiens (human) 9108 MTMR7
  • MGI:6194238
DOID:0060740 methylmalonic aciduria due to methylmalonyl-CoA mutase deficiency HGNC:7526 Homo sapiens (human) 4594 MMUT
  • MGI:6194238
  • PMID:27167370
  • RGD:7240710
DOID:14749 methylmalonic acidemia HGNC:7526 Homo sapiens (human) 4594 MMUT
  • MGI:6194238
DOID:5517 stomach carcinoma HGNC:7527 Homo sapiens (human) 4595 MUTYH
  • PMID:15273732
DOID:0080410 familial adenomatous polyposis 2 HGNC:7527 Homo sapiens (human) 4595 MUTYH
  • RGD:7240710
DOID:0050424 familial adenomatous polyposis HGNC:7527 Homo sapiens (human) 4595 MUTYH
  • PMID:11818965

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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