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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 October 9, 2024
Displaying entries 70601 - 70625 of 71927 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID ▲ Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:0110345 osteogenesis imperfecta type 16 HGNC:18856 Homo sapiens (human) 90993 CREB3L1
  • RGD:7240710
DOID:10534 stomach cancer HGNC:172 Homo sapiens (human) 91 ACVR1B
  • PMID:32066878
DOID:1793 pancreatic cancer HGNC:172 Homo sapiens (human) 91 ACVR1B
  • PMID:11248065
  • PMID:9714055
  • RGD:7240710
DOID:3908 lung non-small cell carcinoma HGNC:172 Homo sapiens (human) 91 ACVR1B
  • PMID:22586632
DOID:5409 lung small cell carcinoma HGNC:172 Homo sapiens (human) 91 ACVR1B
  • PMID:33880365
DOID:1790 malignant mesothelioma HGNC:172 Homo sapiens (human) 91 ACVR1B
  • PMID:30061637
DOID:7004 ACTH-secreting pituitary adenoma HGNC:12631 Homo sapiens (human) 9101 USP8
  • RGD:7240710
DOID:9074 systemic lupus erythematosus HGNC:15626 Homo sapiens (human) 9103 FCGR2C
  • MGI:6194238
DOID:12365 malaria HGNC:15626 Homo sapiens (human) 9103 FCGR2C
  • MGI:6194238
DOID:1168 familial hyperlipidemia HGNC:9989 Homo sapiens (human) 9104 RGN
  • MGI:6194238
DOID:684 hepatocellular carcinoma HGNC:9989 Homo sapiens (human) 9104 RGN
  • MGI:6194238
DOID:10534 stomach cancer HGNC:9989 Homo sapiens (human) 9104 RGN
  • PMID:28035468
DOID:0111225 centronuclear myopathy X-linked HGNC:7453 Homo sapiens (human) 9107 MTMR6
  • MGI:6194238
DOID:14717 centronuclear myopathy HGNC:7453 Homo sapiens (human) 9107 MTMR6
  • MGI:6194238
DOID:10595 Charcot-Marie-Tooth disease HGNC:7453 Homo sapiens (human) 9107 MTMR6
  • MGI:6194238
DOID:10595 Charcot-Marie-Tooth disease HGNC:7454 Homo sapiens (human) 9108 MTMR7
  • MGI:6194238
DOID:0111225 centronuclear myopathy X-linked HGNC:7454 Homo sapiens (human) 9108 MTMR7
  • MGI:6194238
DOID:14717 centronuclear myopathy HGNC:7454 Homo sapiens (human) 9108 MTMR7
  • 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:0111225 centronuclear myopathy X-linked HGNC:7452 Homo sapiens (human) 9110 MTMR4
  • MGI:6194238
DOID:305 carcinoma HGNC:6514 Homo sapiens (human) 9113 LATS1
  • MGI:6194238
DOID:162 cancer HGNC:6514 Homo sapiens (human) 9113 LATS1
  • MGI:6194238
DOID:263 kidney cancer HGNC:6514 Homo sapiens (human) 9113 LATS1
  • MGI:6194238
DOID:898 autosomal dominant polycystic kidney disease HGNC:6514 Homo sapiens (human) 9113 LATS1
  • 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: December 9, 2024