Gene table: search width pubmed_id = 29878067


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Disease phenotype
Item
in
this
table
Key
references
Gene symbol (chromosome)

protein
All allelic disease phenotypes - locus/disease symbols
Spinocerebellar ataxia 42, early-onset, severe, with neurodevelopmental deficits - (AD)
13.39
29878067
CACNA1G (17q21.33)
calcium voltage-gated channel subunit alpha1 G
* Spinocerebellar ataxia 42 - SCA42
* Spinocerebellar ataxia 42, early-onset, severe, with neurodevelopmental deficits - SCA42ND