Identity
HGNC
LOCATION
11q23.3
LOCUSID
ALIAS
DFNA12,DFNA8,DFNB21
FUSION GENES
Non-annotated gene. Preliminary data : if you are an author who wish to write a full paper/card on this gene, contribute in submission tool
Other Information
Locus ID:
NCBI: 7007
MIM: 602574
HGNC: 11720
Ensembl: ENSG00000109927
Variants:
dbSNP: 7007
ClinVar: 7007
TCGA: ENSG00000109927
COSMIC: TECTA
RNA/Proteins
| Gene ID | Transcript ID | Uniprot |
|---|---|---|
| ENSG00000109927 | ENST00000264037 | O75443 |
| ENSG00000109927 | ENST00000392793 | O75443 |
| ENSG00000109927 | ENST00000642222 | A0A2R8YDL0 |
| ENSG00000109927 | ENST00000645008 | A0A2R8YGQ5 |
Expression (GTEx)
Pathways
Protein levels (Protein atlas)
References
| Pubmed ID | Year | Title | Citations |
|---|---|---|---|
| 35870179 | 2022 | Characterization of a possible founder synonymous variant in TECTA in multiple individuals with autosomal recessive hearing loss. | 0 |
| 35870179 | 2022 | Characterization of a possible founder synonymous variant in TECTA in multiple individuals with autosomal recessive hearing loss. | 0 |
| 33976695 | 2021 | Next-Generation Sequencing Identifies Pathogenic Variants in HGF, POU3F4, TECTA, and MYO7A in Consanguineous Pakistani Deaf Families. | 2 |
| 33976695 | 2021 | Next-Generation Sequencing Identifies Pathogenic Variants in HGF, POU3F4, TECTA, and MYO7A in Consanguineous Pakistani Deaf Families. | 2 |
| 32382995 | 2020 | A comparative analysis of genetic hearing loss phenotypes in European/American and Japanese populations. | 12 |
| 32382995 | 2020 | A comparative analysis of genetic hearing loss phenotypes in European/American and Japanese populations. | 12 |
| 30703234 | 2019 | [Diagnosis and reproductive guidance for a couple carrying a novel c.1893C>T mutation of the TECTA gene]. | 0 |
| 30703234 | 2019 | [Diagnosis and reproductive guidance for a couple carrying a novel c.1893C>T mutation of the TECTA gene]. | 0 |
| 28012541 | 2017 | A novel TECTA mutation causes ARNSHL. | 8 |
| 28946916 | 2017 | Prevalence of TECTA mutation in patients with mid-frequency sensorineural hearing loss. | 11 |
| 28012541 | 2017 | A novel TECTA mutation causes ARNSHL. | 8 |
| 28946916 | 2017 | Prevalence of TECTA mutation in patients with mid-frequency sensorineural hearing loss. | 11 |
| 27142990 | 2016 | Research progress in pathogenic genes of hereditary non-syndromic mid-frequency deafness. | 6 |
| 27368438 | 2016 | A novel biallelic splice site mutation of TECTA causes moderate to severe hearing impairment in an Algerian family. | 7 |
| 27142990 | 2016 | Research 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)
