rs948588947
This variant is located in the TNIK gene.
▶ClinVar annotation
About TNIK
Wnt signaling plays important roles in carcinogenesis and embryonic development. The protein encoded by this gene is a serine/threonine kinase that functions as an activator of the Wnt signaling pathway. Mutations in this gene are associated with an autosomal recessive form of cognitive disability. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Jul 2017]
View all TNIK variants →Gene information from NCBI Gene. Variant classifications from ClinVar.
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