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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 9776 - 9800 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID ▲ Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:0111313 idiopathic generalized epilepsy 12 HGNC:11005 Homo sapiens (human) 6513 SLC2A1
  • RGD:7240710
DOID:1459 hypothyroidism HGNC:11005 Homo sapiens (human) 6513 SLC2A1
  • MGI:6194238
DOID:9352 type 2 diabetes mellitus HGNC:11005 Homo sapiens (human) 6513 SLC2A1
  • PMID:18613291
  • PMID:7516306
  • PMID:9789717
DOID:1825 childhood absence epilepsy HGNC:11005 Homo sapiens (human) 6513 SLC2A1
  • PMID:26537434
DOID:255 hemangioma HGNC:11005 Homo sapiens (human) 6513 SLC2A1
  • PMID:10665907
DOID:10652 Alzheimer's disease HGNC:11005 Homo sapiens (human) 6513 SLC2A1
  • PMID:8179300
DOID:9970 obesity HGNC:11005 Homo sapiens (human) 6513 SLC2A1
  • PMID:24842895
DOID:5577 gastrinoma HGNC:11006 Homo sapiens (human) 6514 SLC2A2
  • PMID:12114701
  • PMID:8421107
DOID:1062 Fanconi syndrome HGNC:11006 Homo sapiens (human) 6514 SLC2A2
  • RGD:7240710
DOID:9352 type 2 diabetes mellitus HGNC:11006 Homo sapiens (human) 6514 SLC2A2
  • MGI:6194238
  • PMID:17636114
  • PMID:8027028
  • RGD:7240710
DOID:3892 insulinoma HGNC:11006 Homo sapiens (human) 6514 SLC2A2
  • PMID:12114701
  • PMID:8421107
DOID:2747 glycogen storage disease HGNC:11006 Homo sapiens (human) 6514 SLC2A2
  • PMID:9354798
DOID:3138 acanthosis nigricans HGNC:11007 Homo sapiens (human) 6515 SLC2A3
  • PMID:11436180
DOID:10763 hypertension HGNC:11007 Homo sapiens (human) 6515 SLC2A3
  • MGI:6194238
DOID:10652 Alzheimer's disease HGNC:11007 Homo sapiens (human) 6515 SLC2A3
  • PMID:8179300
DOID:9351 diabetes mellitus HGNC:11007 Homo sapiens (human) 6515 SLC2A3
  • PMID:10086067
DOID:9352 type 2 diabetes mellitus HGNC:11007 Homo sapiens (human) 6515 SLC2A3
  • PMID:19110659
DOID:83 cataract HGNC:11007 Homo sapiens (human) 6515 SLC2A3
  • MGI:6194238
DOID:2747 glycogen storage disease RGD:68419 Rattus norvegicus (Norway rat) 65152 Pfkm
  • MGI:6194238
DOID:11721 glycogen storage disease VII RGD:68419 Rattus norvegicus (Norway rat) 65152 Pfkm
  • MGI:6194238
DOID:0014667 disease of metabolism RGD:68419 Rattus norvegicus (Norway rat) 65152 Pfkm
  • MGI:6194238
DOID:9352 type 2 diabetes mellitus HGNC:11009 Homo sapiens (human) 6517 SLC2A4
  • MGI:6194238
  • PMID:1918382
DOID:6000 congestive heart failure HGNC:11009 Homo sapiens (human) 6517 SLC2A4
  • PMID:18778861
DOID:3393 coronary artery disease HGNC:11009 Homo sapiens (human) 6517 SLC2A4
  • PMID:21645024
DOID:6432 pulmonary hypertension HGNC:11009 Homo sapiens (human) 6517 SLC2A4
  • 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