Skip to content
GeneQ18031940· pop 7· linked from 142 articles

Also known as DFNA12, DFNA8, DFNB21, tectorin alpha

Alpha-tectorin is a protein that in humans is encoded by the TECTA gene.

Gene data

TECTA
Name
tectorin alpha
Type
protein-coding
Position
121,101,243–121,191,490 (+)
Aliases
DFNA12, DFNA8, DFNB21
RefSeq RNA
NM_005422.4
RefSeq protein
NP_005413.2

The tectorial membrane is an extracellular matrix of the inner ear that contacts the stereocilia bundles of specialized sensory hair cells. Sound induces movement of these hair cells relative to the tectorial membrane, deflects the stereocilia, and leads to fluctuations in hair-cell membrane potential, transducing sound into electrical signals. Alpha-tectorin is one of the major noncollagenous components of the tectorial membrane. Mutations in the TECTA gene have been shown to be responsible for autosomal dominant nonsyndromic hearing impairment and a recessive form of sensorineural pre-lingual non-syndromic deafness. [provided by RefSeq, Jul 2008].

via MyGene.info

Gene · Ensembl

tectorin alpha

Symbol
TECTA
Biotype
Protein coding
Organism
Homo sapiens
Location
11:121,101,243-121,191,490
Strand
Forward (+)
Assembly
GRCh38
View on Ensembl →

via Ensembl · EMBL-EBI

Wikidata facts

Show 5 more facts
HomoloGene ID
3955
genomic end
121191490
genomic start
121101243
cytogenetic location
11q23.3
Sources (7)

via Wikidata · CC0

~1 min read

Article

2 sections
Contents
  • References
  • Further reading

Alpha-tectorin is a protein that in humans is encoded by the TECTA gene.

The tectorial membrane is an apical extracellular matrix (aECM) of the inner ear that contacts the stereocilia bundles of specialized sensory hair cells. Sound induces movement of these hair cells relative to the tectorial membrane, deflects the stereocilia, and leads to fluctuations in hair-cell membrane potential, transducing sound into electrical signals. Alpha-tectorin is one of the major noncollagenous components of the tectorial membrane. Mutations in the TECTA gene have been shown to be responsible for autosomal dominant nonsyndromic hearing impairment and a recessive form of sensorineural pre-lingual non-syndromic deafness.

Available in 7 languages

via Wikidata sitelinks · CC0

Connections

Categories