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Gene entry

TECTA

tectorin alpha

Chromosome
11
Cytoband
11q23.3
Variants (rsID)
49

TECTA is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 11 (region 11q23.3). Its official name is “tectorin alpha”. The reference table lists 49 variants (rsID) for this gene.

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Clinically classified variants

24 reference-table entries with clinical significance.

  • rs520805Benignsingle nucleotide variantAutosomal recessive nonsyndromic hearing loss 21|Autosomal dominant nonsyndromic hearing loss 12
  • rs111759871Conflicting interpretationssingle nucleotide variantAutosomal dominant nonsyndromic hearing loss 12
  • rs138477419Conflicting interpretationssingle nucleotide variantAutosomal recessive nonsyndromic hearing loss 21|Autosomal dominant nonsyndromic hearing loss 12
  • rs140236996Conflicting interpretationssingle nucleotide variantAutosomal dominant nonsyndromic hearing loss 12|Autosomal recessive nonsyndromic hearing loss 21|Inborn genetic diseases|Rare genetic deafness|Sensorineural hearing loss disorder
  • rs144844263Conflicting interpretationssingle nucleotide variantAutosomal dominant nonsyndromic hearing loss 12|Autosomal recessive nonsyndromic hearing loss 21
  • rs186780639Conflicting interpretationssingle nucleotide variantAutosomal dominant nonsyndromic hearing loss 12|Autosomal recessive nonsyndromic hearing loss 21
  • rs200821009Conflicting interpretationssingle nucleotide variant
  • rs202199158Conflicting interpretationssingle nucleotide variantAutosomal recessive nonsyndromic hearing loss 21|Autosomal dominant nonsyndromic hearing loss 12
  • rs33981325Conflicting interpretationssingle nucleotide variantAutosomal recessive nonsyndromic hearing loss 21|Autosomal dominant nonsyndromic hearing loss 12
  • rs367974065Conflicting interpretationssingle nucleotide variantAutosomal recessive nonsyndromic hearing loss 21|Autosomal dominant nonsyndromic hearing loss 12
  • rs139165033Likely benignsingle nucleotide variantAutosomal dominant nonsyndromic hearing loss 12|Autosomal recessive nonsyndromic hearing loss 21|Nonsyndromic genetic hearing loss|Hearing impairment
  • rs142486386Likely benignsingle nucleotide variantNonsyndromic genetic hearing loss
  • rs144012985Likely benignsingle nucleotide variantAutosomal recessive nonsyndromic hearing loss 21|Autosomal dominant nonsyndromic hearing loss 12|Nonsyndromic genetic hearing loss
  • rs144343770Likely benignsingle nucleotide variantAutosomal recessive nonsyndromic hearing loss 21|Autosomal dominant nonsyndromic hearing loss 12|Nonsyndromic genetic hearing loss
  • rs144682235Likely benignsingle nucleotide variantAutosomal dominant nonsyndromic hearing loss 12|Autosomal recessive nonsyndromic hearing loss 21|Nonsyndromic genetic hearing loss
  • rs368627411Likely benignsingle nucleotide variantNonsyndromic genetic hearing loss
  • rs267607107Othersingle nucleotide variantDeafness, Autosomal Dominant 12
  • rs281865415Othersingle nucleotide variantDeafness, Autosomal Dominant 12
  • rs121909059Pathogenicsingle nucleotide variantAutosomal dominant nonsyndromic hearing loss 12
  • rs146175803Uncertain significancesingle nucleotide variantAutosomal dominant nonsyndromic hearing loss 12|Autosomal recessive nonsyndromic hearing loss 21
  • rs147890616Uncertain significancesingle nucleotide variantAutosomal dominant nonsyndromic hearing loss 12|Autosomal recessive nonsyndromic hearing loss 21|Autosomal dominant nonsyndromic hearing loss 12|Autosomal recessive nonsyndromic hearing loss 21
  • rs148440178Uncertain significancesingle nucleotide variantAutosomal recessive nonsyndromic hearing loss 21|Autosomal dominant nonsyndromic hearing loss 12
  • rs192787819Uncertain significancesingle nucleotide variant
  • rs201860044Uncertain significancesingle nucleotide variant

Other listed variants

Public references

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