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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 10626 - 10650 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID ▼ Species Gene ID Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:0060326 myelomeningocele HGNC:11005 Homo sapiens (human) 6513 SLC2A1
  • PMID:21135204
  • PMID:23427181
DOID:2978 carbohydrate metabolic disorder HGNC:11005 Homo sapiens (human) 6513 SLC2A1
  • PMID:20382060
  • PMID:22011817
  • PMID:9462754
  • RGD:7240710
DOID:10763 hypertension HGNC:11005 Homo sapiens (human) 6513 SLC2A1
  • MGI:6194238
DOID:0090045 childhood onset GLUT1 deficiency syndrome 2 HGNC:11005 Homo sapiens (human) 6513 SLC2A1
  • RGD:7240710
DOID:2154 nephroblastoma HGNC:11005 Homo sapiens (human) 6513 SLC2A1
  • PMID:22483234
DOID:3525 middle cerebral artery infarction HGNC:11005 Homo sapiens (human) 6513 SLC2A1
  • MGI:6194238
DOID:10591 pre-eclampsia HGNC:11005 Homo sapiens (human) 6513 SLC2A1
  • PMID:22840297
DOID:10487 Hirschsprung's disease HGNC:11005 Homo sapiens (human) 6513 SLC2A1
  • PMID:10975929
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:14687 diastrophic dysplasia HGNC:10994 Homo sapiens (human) 1836 SLC26A2
  • MGI:6194238
  • PMID:10482955
  • RGD:7240710
DOID:676 juvenile rheumatoid arthritis HGNC:10994 Homo sapiens (human) 1836 SLC26A2
  • PMID:17393463
DOID:0070300 multiple epiphyseal dysplasia 4 HGNC:10994 Homo sapiens (human) 1836 SLC26A2
  • PMID:24598000
  • RGD:7240710
DOID:0050648 atelosteogenesis HGNC:10994 Homo sapiens (human) 1836 SLC26A2
  • RGD:7240710
DOID:2256 osteochondrodysplasia HGNC:10994 Homo sapiens (human) 1836 SLC26A2
  • PMID:8571951
DOID:0050581 brachydactyly HGNC:10994 Homo sapiens (human) 1836 SLC26A2
  • PMID:21155763
DOID:0080055 achondrogenesis type IB HGNC:10994 Homo sapiens (human) 1836 SLC26A2
  • PMID:8528239
  • RGD:7240710
DOID:2300 spondylolysis HGNC:10994 Homo sapiens (human) 1836 SLC26A2
  • PMID:26077908
DOID:0070341 neonatal-onset type II citrullinemia HGNC:10983 Homo sapiens (human) 10165 SLC25A13
  • RGD:7240710
DOID:9273 citrullinemia HGNC:10983 Homo sapiens (human) 10165 SLC25A13
  • MGI:6194238

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GlyCosmos is a member of the GlySpace Alliance together with GlyGen and Glycomics@ExPASy.

Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

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


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