KCTD19 Chromosome 16

Potassium channel tetramerization domain containing 19

1 variant 1 Health Risk

Upload your DNA to see your personal genotypes for variants in KCTD19.

What This Gene Does

Predicted to enable identical protein binding activity. Predicted to be involved in male meiotic nuclear division. Predicted to be located in nucleus. [provided by Alliance of Genome Resources, Jul 2025]

Gene Info

Gene Group

KCTD family

Locus Type

gene with protein product

Location

16q22.1

Ensembl

ENSG00000168676

Associated Conditions (1)

Cerebral visual impairment and intellectual disability

Key Variants

RS869312866

Likely pathogenic

Cerebral visual impairment and intellectual disability, Cerebral visual impairment and intellectual disability

Health Risk

All Variants (1)

RSID	Category	Clinical Significance	Conditions
RS869312866	Health Risk	Likely pathogenic	Cerebral visual impairment and intellectual disability, Cerebral visual impairment and intellectual disability