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FLASH GENE

Symbol

CNTN6

contributors: mct/npt - updated : 27-09-2022

HGNC name	contactin 6
HGNC id	2176

FLASH GENE DNA RNA EXPRESSION PROTEIN DISORDER ANIMAL & CELL MODELS

ASSOCIATED DISORDERS

corresponding disease(s)

Susceptibility

to abnormal auditory sensory perception in autism spectrum disorders

Variant & Polymorphism other	CNTN6 mutations are risk factors for abnormal auditory sensory perception in autism spectrum disorders

Candidate gene

Marker

Therapy target

ANIMAL & CELL MODELS

Cntn6 is expressed in the developing hippocampus, and its deficiency in mice affects spatial learning and memory