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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 2201 - 2225 of 12216 in total
Disease ID ▲ Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:0081326 oxoglutarate dehydrogenase deficiency MGI:1098267 Mus musculus (house mouse) 18293 Ogdh
  • MGI:6194238
DOID:0081326 oxoglutarate dehydrogenase deficiency HGNC:8124 Homo sapiens (human) 4967 OGDH
  • MGI:6194238
  • RGD:7240710
DOID:0081326 oxoglutarate dehydrogenase deficiency WB:WBGene00020679 Caenorhabditis elegans 177235 ogdh-1
  • MGI:6194238
DOID:0081326 oxoglutarate dehydrogenase deficiency HGNC:25590 Homo sapiens (human) 55753 OGDHL
  • MGI:6194238
DOID:0081330 glycogen storage disease Ib HGNC:4061 Homo sapiens (human) 2542 SLC37A4
  • PMID:9428641
  • RGD:7240710
DOID:0081331 glycogen storage disease Ic HGNC:4061 Homo sapiens (human) 2542 SLC37A4
  • RGD:7240710
DOID:0081337 congenital myopathy HGNC:9639 Homo sapiens (human) 9200 HACD1
  • RGD:7240710
DOID:0081376 obsolete sorbitol dehydrogenase deficiency with peripheral neuropathy MGI:98266 Mus musculus (house mouse) 20322 Sord
  • MGI:6194238
DOID:0081376 obsolete sorbitol dehydrogenase deficiency with peripheral neuropathy SGD:S000002405 Saccharomyces cerevisiae S288C 851351 SOR2
  • MGI:6194238
DOID:0081376 obsolete sorbitol dehydrogenase deficiency with peripheral neuropathy HGNC:11184 Homo sapiens (human) 6652 SORD
  • MGI:6194238
DOID:0081376 obsolete sorbitol dehydrogenase deficiency with peripheral neuropathy RGD:3734 Rattus norvegicus (Norway rat) 24788 Sord
  • MGI:6194238
DOID:0081376 obsolete sorbitol dehydrogenase deficiency with peripheral neuropathy SGD:S000004060 Saccharomyces cerevisiae S288C 850759 XYL2
  • MGI:6194238
DOID:0081376 obsolete sorbitol dehydrogenase deficiency with peripheral neuropathy SGD:S000003920 Saccharomyces cerevisiae S288C 853624 SOR1
  • MGI:6194238
DOID:0081381 juvenile amyotrophic lateral sclerosis type 27 HGNC:11277 Homo sapiens (human) 10558 SPTLC1
  • RGD:7240710
DOID:0081385 ataxia-telangiectasia-like disorder-2 RGD:3269 Rattus norvegicus (Norway rat) 25737 Pcna
  • MGI:6194238
DOID:0081385 ataxia-telangiectasia-like disorder-2 MGI:97503 Mus musculus (house mouse) 18538 Pcna
  • MGI:6194238
DOID:0081385 ataxia-telangiectasia-like disorder-2 HGNC:8729 Homo sapiens (human) 5111 PCNA
  • RGD:7240710
DOID:0081419 childhood-onset dystonia with optic atrophy and basal ganglia abnormalities HGNC:19691 Homo sapiens (human) 51102 MECR
  • RGD:7240710
DOID:0081427 autosomal recessive distal hereditary motor neuronopathy 8 RGD:3734 Rattus norvegicus (Norway rat) 24788 Sord
  • MGI:6194238
DOID:0081427 autosomal recessive distal hereditary motor neuronopathy 8 SGD:S000002405 Saccharomyces cerevisiae S288C 851351 SOR2
  • MGI:6194238
DOID:0081427 autosomal recessive distal hereditary motor neuronopathy 8 SGD:S000004060 Saccharomyces cerevisiae S288C 850759 XYL2
  • MGI:6194238
DOID:0081427 autosomal recessive distal hereditary motor neuronopathy 8 SGD:S000003920 Saccharomyces cerevisiae S288C 853624 SOR1
  • MGI:6194238
DOID:0081427 autosomal recessive distal hereditary motor neuronopathy 8 MGI:98266 Mus musculus (house mouse) 20322 Sord
  • MGI:6194238
DOID:0081427 autosomal recessive distal hereditary motor neuronopathy 8 HGNC:11184 Homo sapiens (human) 6652 SORD
  • RGD:7240710
DOID:0090001 Fraser syndrome HGNC:23399 Homo sapiens (human) 158326 FREM1
  • MGI:6194238

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Supported by JST NBDC Grant Number JPMJND2204

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


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