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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 9426 - 9450 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID ▼ Species Gene ID Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:0111240 congenital muscular dystrophy-dystroglycanopathy type A2 HGNC:19743 Homo sapiens (human) 29954 POMT2
  • RGD:7240710
DOID:0112374 muscular dystrophy-dystroglycanopathy HGNC:19743 Homo sapiens (human) 29954 POMT2
  • MGI:6194238
DOID:9884 muscular dystrophy HGNC:19743 Homo sapiens (human) 29954 POMT2
  • PMID:17634419
DOID:0110298 autosomal recessive limb-girdle muscular dystrophy type 2N HGNC:19743 Homo sapiens (human) 29954 POMT2
  • RGD:7240710
DOID:0050560 Walker-Warburg syndrome HGNC:19743 Homo sapiens (human) 29954 POMT2
  • MGI:6194238
  • PMID:15894594
DOID:0112380 muscular dystrophy-dystroglycanopathy type B2 HGNC:19743 Homo sapiens (human) 29954 POMT2
  • RGD:7240710
DOID:0110274 autosomal recessive limb-girdle muscular dystrophy HGNC:19743 Homo sapiens (human) 29954 POMT2
  • PMID:17923109
DOID:0050453 lissencephaly HGNC:19743 Homo sapiens (human) 29954 POMT2
  • PMID:17559086
DOID:5419 schizophrenia HGNC:1971 Homo sapiens (human) 9469 CHST3
  • MGI:6194238
DOID:2256 osteochondrodysplasia HGNC:1971 Homo sapiens (human) 9469 CHST3
  • PMID:15215498
DOID:0050813 spondyloepiphyseal dysplasia with congenital joint dislocations HGNC:1971 Homo sapiens (human) 9469 CHST3
  • RGD:7240710
DOID:0081419 childhood-onset dystonia with optic atrophy and basal ganglia abnormalities HGNC:19691 Homo sapiens (human) 51102 MECR
  • RGD:7240710
DOID:0111756 Leber hereditary optic neuropathy with demyelinating disease of CNS HGNC:19691 Homo sapiens (human) 51102 MECR
  • MGI:6194238
DOID:5723 optic atrophy HGNC:19691 Homo sapiens (human) 51102 MECR
  • RGD:7240710
DOID:0111156 spermatogenic failure 9 HGNC:19414 Homo sapiens (human) 283417 DPY19L2
  • RGD:7240710
DOID:8619 recurrent hypersomnia HGNC:1938 Homo sapiens (human) 1120 CHKB
  • PMID:19404393
DOID:8986 narcolepsy HGNC:1938 Homo sapiens (human) 1120 CHKB
  • PMID:18820697
DOID:9884 muscular dystrophy HGNC:1938 Homo sapiens (human) 1120 CHKB
  • PMID:21665002
DOID:10907 microcephaly HGNC:1938 Homo sapiens (human) 1120 CHKB
  • MGI:6194238
DOID:0110632 megaconial type congenital muscular dystrophy HGNC:1938 Homo sapiens (human) 1120 CHKB
  • MGI:6194238
  • RGD:7240710
DOID:1059 intellectual disability HGNC:1938 Homo sapiens (human) 1120 CHKB
  • PMID:21665002
DOID:1826 epilepsy HGNC:1938 Homo sapiens (human) 1120 CHKB
  • MGI:6194238
DOID:1826 epilepsy HGNC:1937 Homo sapiens (human) 1119 CHKA
  • MGI:6194238
DOID:224 transient cerebral ischemia HGNC:1937 Homo sapiens (human) 1119 CHKA
  • MGI:6194238
DOID:219 colon cancer HGNC:1937 Homo sapiens (human) 1119 CHKA
  • 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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Last updated: August 19, 2024