Identity
HGNC
LOCATION
16p12.2
LOCUSID
ALIAS
CT108,DFNB22
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: 146183
MIM: 607038
HGNC: 16378
Ensembl: ENSG00000155719
Variants:
dbSNP: 146183
ClinVar: 146183
TCGA: ENSG00000155719
COSMIC: OTOA
RNA/Proteins
Expression (GTEx)
Pathways
Protein levels (Protein atlas)
References
| Pubmed ID | Year | Title | Citations |
|---|---|---|---|
| 37114731 | 2023 | [Phenotype-genotype analysis of the autosomal recessive hereditary hearing loss caused by OTOA variations]. | 0 |
| 37114731 | 2023 | [Phenotype-genotype analysis of the autosomal recessive hereditary hearing loss caused by OTOA variations]. | 0 |
| 33492714 | 2021 | Molecular characterization of pathogenic OTOA gene conversions in hearing loss patients. | 7 |
| 33492714 | 2021 | Molecular characterization of pathogenic OTOA gene conversions in hearing loss patients. | 7 |
| 32552051 | 2020 | Polymorphisms in Neuronal Growth Regulator 1 and Otoancorin Alternate the Susceptibility to Lung Cancer in Chinese Nonsmoking Females. | 0 |
| 32552051 | 2020 | Polymorphisms in Neuronal Growth Regulator 1 and Otoancorin Alternate the Susceptibility to Lung Cancer in Chinese Nonsmoking Females. | 0 |
| 30740825 | 2019 | Clarification of glycosylphosphatidylinositol anchorage of OTOANCORIN and human OTOA variants associated with deafness. | 6 |
| 30740825 | 2019 | Clarification of glycosylphosphatidylinositol anchorage of OTOANCORIN and human OTOA variants associated with deafness. | 6 |
| 29178603 | 2018 | Targeted next-generation sequencing and parental genotyping in sporadic Chinese Han deaf patients. | 9 |
| 29178603 | 2018 | Targeted next-generation sequencing and parental genotyping in sporadic Chinese Han deaf patients. | 9 |
| 23173898 | 2013 | Novel OTOA mutations cause autosomal recessive non-syndromic hearing impairment in Pakistani families. | 8 |
| 23173898 | 2013 | Novel OTOA mutations cause autosomal recessive non-syndromic hearing impairment in Pakistani families. | 8 |
| 19888295 | 2010 | Five novel loci for inherited hearing loss mapped by SNP-based homozygosity profiles in Palestinian families. | 42 |
| 20379614 | 2010 | Personalized smoking cessation: interactions between nicotine dose, dependence and quit-success genotype score. | 78 |
| 19888295 | 2010 | Five novel loci for inherited hearing loss mapped by SNP-based homozygosity profiles in Palestinian families. | 42 |
Citation
Dessen P
OTOA (otoancorin)
Atlas Genet Cytogenet Oncol Haematol. 2014-11-01
Online version: http://atlasgeneticsoncology.org/gene/71572/otoa-(otoancorin)
