autosomal dominant intellectual developmental disorder 10

Summary
Synonym
  • MRD10
  • autosomal dominant mental retardation 10
  • autosomal dominant non-syndromic intellectual disability 10
Definition
An autosomal dominant intellectual developmental disorder that has_material_basis_in an autosomal dominant mutation of the CACNG2 gene on chromosome 22q12.3.
Super Class
autosomal dominant intellectual developmental disorder
Disease Ontology
DOID:0070040
Mondo Disease Ontology
OMIM
Related Genes
Displaying 1 entry
Gene ID Gene Symbol Description Source
10369 CACNG2 calcium voltage-gated channel auxiliary subunit gamma 2
Displaying 1 entry
Gene ID Gene Symbol Description Source
12300 Cacng2 calcium channel, voltage-dependent, gamma subunit 2
Displaying 1 entry
Gene ID Gene Symbol Description Source
84347 Cacng2 calcium voltage-gated channel auxiliary subunit gamma 2

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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