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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 64051 - 64075 of 71927 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol ▼ FlyGlycoDB Evidence Code Names References
DOID:11723 Duchenne muscular dystrophy HGNC:1390 Homo sapiens (human) 775 CACNA1C
  • MGI:6194238
DOID:0110220 Brugada syndrome 3 HGNC:1390 Homo sapiens (human) 775 CACNA1C
  • RGD:7240710
DOID:0050214 Lambert-Eaton myasthenic syndrome HGNC:1389 Homo sapiens (human) 774 CACNA1B
  • PMID:16289869
DOID:1826 epilepsy HGNC:1389 Homo sapiens (human) 774 CACNA1B
  • MGI:6194238
DOID:6364 migraine HGNC:1389 Homo sapiens (human) 774 CACNA1B
  • MGI:6194238
DOID:0111181 familial hemiplegic migraine 1 HGNC:1389 Homo sapiens (human) 774 CACNA1B
  • MGI:6194238
DOID:2377 multiple sclerosis HGNC:1389 Homo sapiens (human) 774 CACNA1B
  • PMID:11353727
DOID:0050951 hereditary ataxia HGNC:1389 Homo sapiens (human) 774 CACNA1B
  • MGI:6194238
DOID:4724 brain edema HGNC:1389 Homo sapiens (human) 774 CACNA1B
  • PMID:27487831
DOID:0111181 familial hemiplegic migraine 1 HGNC:1388 Homo sapiens (human) 773 CACNA1A
  • MGI:6194238
  • RGD:7240710
DOID:10024 migraine with aura HGNC:1388 Homo sapiens (human) 773 CACNA1A
  • PMID:10408532
DOID:0060178 familial hemiplegic migraine HGNC:1388 Homo sapiens (human) 773 CACNA1A
  • MGI:6194238
DOID:6364 migraine HGNC:1388 Homo sapiens (human) 773 CACNA1A
  • MGI:6194238
  • PMID:24108129
DOID:1825 childhood absence epilepsy HGNC:1388 Homo sapiens (human) 773 CACNA1A
  • MGI:6194238
DOID:0070309 absence epilepsy HGNC:1388 Homo sapiens (human) 773 CACNA1A
  • MGI:6194238
DOID:0050951 hereditary ataxia HGNC:1388 Homo sapiens (human) 773 CACNA1A
  • MGI:6194238
DOID:0050753 cerebellar ataxia HGNC:1388 Homo sapiens (human) 773 CACNA1A
  • MGI:6194238
DOID:0050214 Lambert-Eaton myasthenic syndrome HGNC:1388 Homo sapiens (human) 773 CACNA1A
  • MGI:6194238
DOID:1826 epilepsy HGNC:1388 Homo sapiens (human) 773 CACNA1A
  • MGI:6194238
DOID:0050956 spinocerebellar ataxia type 6 HGNC:1388 Homo sapiens (human) 773 CACNA1A
  • MGI:6194238
  • RGD:7240710
DOID:3328 temporal lobe epilepsy HGNC:1388 Homo sapiens (human) 773 CACNA1A
  • MGI:6194238
DOID:0050990 episodic ataxia type 2 HGNC:1388 Homo sapiens (human) 773 CACNA1A
  • MGI:6194238
  • PMID:14530926
  • RGD:7240710
DOID:0050835 generalized dystonia HGNC:1388 Homo sapiens (human) 773 CACNA1A
  • MGI:6194238
DOID:0080454 developmental and epileptic encephalopathy 42 HGNC:1388 Homo sapiens (human) 773 CACNA1A
  • RGD:7240710
DOID:0050704 childhood electroclinical syndrome HGNC:1388 Homo sapiens (human) 773 CACNA1A
  • 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: December 9, 2024