Gene entry

TCTN3

tectonic family member 3

Chromosome: 10
Cytoband: 10q24.1
Variants (rsID): 6

TCTN3 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 10 (region 10q24.1). Its official name is “tectonic family member 3”. The reference table lists 6 variants (rsID) for this gene.

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Clinically classified variants

3 reference-table entries with clinical significance.

rs11553577Benignsingle nucleotide variantOrofacial-digital syndrome IV|Joubert syndrome 18
rs141088838Benignsingle nucleotide variantOrofacial-digital syndrome IV|Joubert syndrome 18
rs55859130Benignsingle nucleotide variantOrofacial-digital syndrome IV|Joubert syndrome 18

Other listed variants

rs12784530
rs41302727
rs201464713

Public references

NCBI Gene
Ensembl
ClinVar

Data from the institutional reference table and public NCBI annotation. For education only; not a substitute for medical or genetic counselling.