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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 October 9, 2024
Displaying entries 65801 - 65825 of 71927 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID ▼ Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:13533 osteopetrosis MGI:103555 Mus musculus (house mouse) 12725 Clcn3
  • MGI:6194238
DOID:0111815 low molecular weight proteinuria with hypercalciuric nephrocalcinosis MGI:103555 Mus musculus (house mouse) 12725 Clcn3
  • MGI:6194238
DOID:0110731 neuronal ceroid lipofuscinosis 3 MGI:103555 Mus musculus (house mouse) 12725 Clcn3
  • PMID:12059962
DOID:0050699 Dent disease MGI:103555 Mus musculus (house mouse) 12725 Clcn3
  • MGI:6194238
DOID:423 myopathy MGI:105061 Mus musculus (house mouse) 12724 Clcn2
  • MGI:6194238
DOID:10579 leukodystrophy MGI:105061 Mus musculus (house mouse) 12724 Clcn2
  • PMID:28859131
DOID:0111312 idiopathic generalized epilepsy 11 MGI:105061 Mus musculus (house mouse) 12724 Clcn2
  • MGI:6194238
DOID:1485 cystic fibrosis MGI:105061 Mus musculus (house mouse) 12724 Clcn2
  • MGI:6194238
DOID:446 primary hyperaldosteronism MGI:105061 Mus musculus (house mouse) 12724 Clcn2
  • MGI:6194238
  • PMID:31727896
DOID:0060019 coronin-1A deficiency MGI:1345961 Mus musculus (house mouse) 12721 Coro1a
  • MGI:6194238
DOID:0090014 severe combined immunodeficiency, autosomal recessive, T cell-negative, B cell-positive, Nk cell-positive MGI:1345961 Mus musculus (house mouse) 12721 Coro1a
  • PMID:18836449
DOID:0080101 Compton-North congenital myopathy HGNC:2171 Homo sapiens (human) 1272 CNTN1
  • MGI:6194238
  • RGD:7240710
DOID:0050741 alcohol dependence HGNC:252 Homo sapiens (human) 127 ADH4
  • PMID:20077761
DOID:2030 anxiety disorder HGNC:2160 Homo sapiens (human) 1269 CNR2
  • MGI:6194238
DOID:4989 pancreatitis HGNC:2160 Homo sapiens (human) 1269 CNR2
  • MGI:6194238
DOID:848 arthritis HGNC:2160 Homo sapiens (human) 1269 CNR2
  • MGI:6194238
DOID:12858 Huntington's disease HGNC:2160 Homo sapiens (human) 1269 CNR2
  • MGI:6194238
DOID:11446 sciatic neuropathy HGNC:2160 Homo sapiens (human) 1269 CNR2
  • MGI:6194238
DOID:750 peptic ulcer disease HGNC:2159 Homo sapiens (human) 1268 CNR1
  • MGI:6194238
DOID:0080855 Parkinsonism HGNC:2159 Homo sapiens (human) 1268 CNR1
  • MGI:6194238
DOID:5419 schizophrenia HGNC:2159 Homo sapiens (human) 1268 CNR1
  • MGI:6194238
  • PMID:11803524
  • PMID:15613777
DOID:2234 focal epilepsy HGNC:2159 Homo sapiens (human) 1268 CNR1
  • MGI:6194238
DOID:9970 obesity HGNC:2159 Homo sapiens (human) 1268 CNR1
  • MGI:6194238
  • PMID:17292652
  • PMID:17405839
  • PMID:31258545
DOID:9352 type 2 diabetes mellitus HGNC:2159 Homo sapiens (human) 1268 CNR1
  • PMID:18678611
DOID:1574 alcohol use disorder HGNC:2159 Homo sapiens (human) 1268 CNR1
  • MGI:6194238

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International Collaboration

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: December 9, 2024