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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 11926 - 11950 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID ▲ Gene Symbol FlyGlycoDB Evidence Code Names References
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: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:1394 urinary schistosomiasis HGNC:1637 Homo sapiens (human) 912 CD1D
  • PMID:22347409
DOID:2957 pulmonary tuberculosis HGNC:1637 Homo sapiens (human) 912 CD1D
  • PMID:30972222
DOID:10534 stomach cancer HGNC:1637 Homo sapiens (human) 912 CD1D
  • PMID:26119195
DOID:12206 dengue hemorrhagic fever HGNC:1637 Homo sapiens (human) 912 CD1D
  • PMID:24945350
DOID:11725 Cornelia de Lange syndrome HGNC:2468 Homo sapiens (human) 9126 SMC3
  • MGI:6194238
DOID:684 hepatocellular carcinoma HGNC:2468 Homo sapiens (human) 9126 SMC3
  • PMID:29996118
DOID:1059 intellectual disability HGNC:2468 Homo sapiens (human) 9126 SMC3
  • PMID:25655089
DOID:0080507 Cornelia de Lange syndrome 3 HGNC:2468 Homo sapiens (human) 9126 SMC3
  • MGI:6194238
  • RGD:7240710
DOID:3083 chronic obstructive pulmonary disease HGNC:5998 Homo sapiens (human) 9173 IL1RL1
  • PMID:19927353
DOID:12662 paracoccidioidomycosis HGNC:5998 Homo sapiens (human) 9173 IL1RL1
  • PMID:28992214
DOID:874 bacterial pneumonia HGNC:5998 Homo sapiens (human) 9173 IL1RL1
  • MGI:6194238
DOID:3393 coronary artery disease HGNC:5998 Homo sapiens (human) 9173 IL1RL1
  • PMID:20602249
DOID:9408 acute myocardial infarction HGNC:5998 Homo sapiens (human) 9173 IL1RL1
  • MGI:6194238
DOID:11266 Hantavirus hemorrhagic fever with renal syndrome HGNC:5998 Homo sapiens (human) 9173 IL1RL1
  • PMID:25658420
DOID:0050156 idiopathic pulmonary fibrosis HGNC:5998 Homo sapiens (human) 9173 IL1RL1
  • PMID:14555548
DOID:4483 rhinitis HGNC:5998 Homo sapiens (human) 9173 IL1RL1
  • PMID:19671251
DOID:12554 hemolytic-uremic syndrome HGNC:5998 Homo sapiens (human) 9173 IL1RL1
  • PMID:30467800

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Supported by JST NBDC Grant Number JPMJND2204

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


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