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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 1376 - 1400 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID ▲ Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:9119 acute myeloid leukemia MGI:95797 Mus musculus (house mouse) 14751 Gpi1
  • MGI:6194238
DOID:1059 intellectual disability MGI:95797 Mus musculus (house mouse) 14751 Gpi1
  • MGI:6194238
DOID:114 heart disease MGI:95797 Mus musculus (house mouse) 14751 Gpi1
  • MGI:6194238
DOID:440 neuromuscular disease MGI:95797 Mus musculus (house mouse) 14751 Gpi1
  • MGI:6194238
DOID:14330 Parkinson's disease MGI:95797 Mus musculus (house mouse) 14751 Gpi1
  • MGI:6194238
DOID:589 congenital hemolytic anemia MGI:95797 Mus musculus (house mouse) 14751 Gpi1
  • MGI:6194238
DOID:2861 congenital nonspherocytic hemolytic anemia MGI:95797 Mus musculus (house mouse) 14751 Gpi1
  • MGI:6194238
  • PMID:8417789
DOID:1574 alcohol use disorder MGI:1342273 Mus musculus (house mouse) 14873 Gsto1
  • MGI:6194238
DOID:10652 Alzheimer's disease MGI:1342273 Mus musculus (house mouse) 14873 Gsto1
  • MGI:6194238
DOID:14330 Parkinson's disease MGI:1342273 Mus musculus (house mouse) 14873 Gsto1
  • MGI:6194238
DOID:0111027 hemochromatosis type 2A HGNC:4887 Homo sapiens (human) 148738 HJV
  • MGI:6194238
  • RGD:7240710
DOID:2352 hemochromatosis HGNC:4887 Homo sapiens (human) 148738 HJV
  • PMID:14647275
DOID:0111230 congenital muscular dystrophy-dystroglycanopathy type A11 HGNC:28596 Homo sapiens (human) 148789 B3GALNT2
  • RGD:7240710
DOID:13810 familial hypercholesterolemia MGI:106594 Mus musculus (house mouse) 14933 Gk
  • MGI:6194238
DOID:0060363 glycerol kinase deficiency MGI:106594 Mus musculus (house mouse) 14933 Gk
  • MGI:6194238
  • PMID:16105550
  • PMID:9302256
DOID:1287 cardiovascular system disease MGI:101805 Mus musculus (house mouse) 14936 Gys1
  • MGI:6194238
DOID:3534 Lafora disease MGI:101805 Mus musculus (house mouse) 14936 Gys1
  • MGI:6194238
DOID:1064 cystinosis HGNC:2518 Homo sapiens (human) 1497 CTNS
  • MGI:6194238
  • PMID:10068513
  • PMID:11565547
  • PMID:18578013
  • PMID:9537412
  • PMID:9792862
  • RGD:7240710
DOID:1062 Fanconi syndrome HGNC:2518 Homo sapiens (human) 1497 CTNS
  • MGI:6194238
DOID:6432 pulmonary hypertension MGI:106590 Mus musculus (house mouse) 15116 Has1
  • MGI:6194238
DOID:3525 middle cerebral artery infarction MGI:107821 Mus musculus (house mouse) 15117 Has2
  • MGI:6194238
DOID:9409 diabetes insipidus MGI:107821 Mus musculus (house mouse) 15117 Has2
  • MGI:6194238
DOID:6432 pulmonary hypertension MGI:107821 Mus musculus (house mouse) 15117 Has2
  • MGI:6194238
DOID:6432 pulmonary hypertension MGI:109599 Mus musculus (house mouse) 15118 Has3
  • MGI:6194238
DOID:3320 Tay-Sachs disease MGI:96073 Mus musculus (house mouse) 15211 Hexa
  • MGI:6194238
  • PMID:7937929
  • PMID:8747922
  • PMID:8789434

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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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Last updated: August 19, 2024