TECTA (tectorin alpha)

2014-01-01  

Identity

HGNC
LOCATION
11q23.3
LOCUSID
ALIAS
DFNA12,DFNA8,DFNB21
FUSION GENES

Other Information

Locus ID:

NCBI: 7007
MIM: 602574
HGNC: 11720
Ensembl: ENSG00000109927

Variants:

dbSNP: 7007
ClinVar: 7007
TCGA: ENSG00000109927
COSMIC: TECTA

RNA/Proteins

Gene IDTranscript IDUniprot
ENSG00000109927ENST00000264037O75443
ENSG00000109927ENST00000392793O75443
ENSG00000109927ENST00000642222A0A2R8YDL0
ENSG00000109927ENST00000645008A0A2R8YGQ5

Expression (GTEx)

0
1
2
3
4

Pathways

PathwaySourceExternal ID
Metabolism of proteinsREACTOMER-HSA-392499
Post-translational protein modificationREACTOMER-HSA-597592
Post-translational modification: synthesis of GPI-anchored proteinsREACTOMER-HSA-163125

Protein levels (Protein atlas)

Not detected
Low
Medium
High

References

Pubmed IDYearTitleCitations
358701792022Characterization of a possible founder synonymous variant in TECTA in multiple individuals with autosomal recessive hearing loss.0
358701792022Characterization of a possible founder synonymous variant in TECTA in multiple individuals with autosomal recessive hearing loss.0
339766952021Next-Generation Sequencing Identifies Pathogenic Variants in HGF, POU3F4, TECTA, and MYO7A in Consanguineous Pakistani Deaf Families.2
339766952021Next-Generation Sequencing Identifies Pathogenic Variants in HGF, POU3F4, TECTA, and MYO7A in Consanguineous Pakistani Deaf Families.2
323829952020A comparative analysis of genetic hearing loss phenotypes in European/American and Japanese populations.12
323829952020A comparative analysis of genetic hearing loss phenotypes in European/American and Japanese populations.12
307032342019[Diagnosis and reproductive guidance for a couple carrying a novel c.1893C>T mutation of the TECTA gene].0
307032342019[Diagnosis and reproductive guidance for a couple carrying a novel c.1893C>T mutation of the TECTA gene].0
280125412017A novel TECTA mutation causes ARNSHL.8
289469162017Prevalence of TECTA mutation in patients with mid-frequency sensorineural hearing loss.11
280125412017A novel TECTA mutation causes ARNSHL.8
289469162017Prevalence of TECTA mutation in patients with mid-frequency sensorineural hearing loss.11
271429902016Research progress in pathogenic genes of hereditary non-syndromic mid-frequency deafness.6
273684382016A novel biallelic splice site mutation of TECTA causes moderate to severe hearing impairment in an Algerian family.7
271429902016Research progress in pathogenic genes of hereditary non-syndromic mid-frequency deafness.6

Citation

Dessen P

TECTA (tectorin alpha)

Atlas Genet Cytogenet Oncol Haematol. 2014-01-01

Online version: http://atlasgeneticsoncology.org/gene/53676/tecta-(tectorin-alpha)