Tectonic Family, Member 3

Alternative Names

  • TCTN3
  • Tectonic 3
  • TECT3
  • Chromosome 10 Open Reading Frame 61
  • C10orf61

Associated Diseases

Joubert Syndrome 18
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OMIM Number

613847

NCBI Gene ID

26123

Uniprot ID

Q6NUS6

Length

30,527 bases

No. of Exons

14

No. of isoforms

5

Protein Name

Tectonic-3

Molecular Mass

66157 Da

Amino Acid Count

607

Genomic Location

chr10:95,663,401-95,693,927

Gene Map Locus
10q24.1

Description

This gene encodes a member of the tectonic gene family which functions in Hedgehog signal transduction and development of the neural tube. Mutations in this gene have been associated with Orofaciodigital Syndrome IV and Joubert Syndrom 18. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [From RefSeq]

Epidemiology in the Arab World

View Map
Variant NameCountryGenomic LocationClinvar Clinical SignificanceCTGA Clinical Significance Condition(s)HGVS ExpressionsdbSNPClinvar
NM_015631.6:c.1437G>CSyria; United Arab Emi...NC_000010.11:g.95682666C>GUncertain SignificanceJoubert Syndrome 18NG_032953.1:g.16478G>C; NM_015631.6:c.1437G>C; NP_056446.4:p.Arg479Ser
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