rs10118726
This variant is located in the TNC gene.
▶ClinVar annotation
Benign★★★☆
4 submitters2 publicationsnot provided; Autosomal dominant nonsyndromic hearing loss 56
View on ClinVar →About TNC
This gene encodes an extracellular matrix protein with a spatially and temporally restricted tissue distribution. This protein is homohexameric with disulfide-linked subunits, and contains multiple EGF-like and fibronectin type-III domains. It is implicated in guidance of migrating neurons as well as axons during development, synaptic plasticity, and neuronal regeneration. [provided by RefSeq, Jul 2011]
View all TNC variants →Gene information from NCBI Gene. Variant classifications from ClinVar.
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