Genes in panel
STRs in panel
Prev Next
Regions in panel
Prev Next

Hearing loss

Gene: CACNG2

Red List (low evidence)

CACNG2 (calcium voltage-gated channel auxiliary subunit gamma 2)
EnsemblGeneIds (GRCh38): ENSG00000166862
EnsemblGeneIds (GRCh37): ENSG00000166862
OMIM: 602911, Gene2Phenotype
CACNG2 is in 2 panels

2 reviews

Maria Bitner-Glindzicz (UCL)

Red List (low evidence)

Jun Shen (Harvard Medical School)

Red List (low evidence)

Mode of inheritance
Unknown

Phenotypes
#614256:Mental retardation, autosomal dominant 10[<omim version=1.0><clinicalSynopsisList>]

Publications

Details

Sources
  • Expert
OMIM
602911
Clinvar variants
Variants in CACNG2
Penetrance
Complete
Panels with this gene

History Filter Activity

24 Jun 2015, Gel status: 0

Added New Source

Ellen McDonagh (Genomics England Curator)

CACNG2 was added to Congenital hearing impairment (Profound/Severe)panel. Sources: Expert