Overview

Variant ID 27335
Entrez Gene ID 7007
Gene TECTA (GeneCards)
Location hg19 11:121010071-121010071
hg38 11:121139362-121139362
Disease Asymptomatic
Method Single cell Sequencing Cell cloning
Mutation(HGVS format) NC_000011.9:g.121010071 G>T (Genome Assembly: GRCh37)

Other information

Exon or Intron NA
Position in protein NA
Amino acid changes in protein NA > NA
Position in cDNA NA
Changes in cDNA NA > NA
mRNA accession NA
mRNA length NA
Reference length 135006516

Annotations and predictions

MAF in gnomAD genome (version 2.0.1) 0
CADD Raw score (version 1.3) -0.428085 (Deleterious)
FATHMM raw prediction score 0.12781 (Tolerated)
Deleterious probability by DeFine 0.1964 (Neutral)
Entrez Gene ID 7007 (NCBI Gene)
Official Gene Symbol TECTA (GeneCards)
Number of variants in TECTA in this database 5 (view all the variants)
Full name tectorin alpha
Band 11q23.3
Other IDs Vega: OTTHUMG00000149908
OMIM: 602574
HGNC: HGNC:11720
Ensembl: ENSG00000109927
Other names DFNA8, DFNA12, DFNB21
Summary 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]

Individual #1

Individual ID 29217587.03 (view all the variants in this individual)
Pubmed ID 29217587
Whose mosaic mutation Normal  
Phenotype 1  
Disease Asymptomatic
OMIM ID