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Gene : OTOA Homo sapiens

Name  ? otoancorin Cytological Location  16p12.2|16p12.2
Brief Description  otoancorin
description  The protein encoded by this gene is specifically expressed in the inner ear, and is located at the interface between the apical surface of the inner ear sensory epithelia and their overlying acellular gels. It is prposed that this protein is involved in the attachment of the inner ear acellular gels to the apical surface of the underlying nonsensory cells. Mutations in this gene are associated with autosomal recessive deafness type 22 (DFNB22). Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Sep 2009]
  • synonyms:
  • DFNB22,
  • NM_001161683,
  • CT108,
  • uc002djh.3,
  • HGNC:16378,
  • cancer/testis antigen 108,
  • deafness, autosomal recessive 22,
  • DFNB22,
  • OTTHUMG00000090721,
  • AK057335,
  • OTOA,
  • CT108
  • identifiers:
  • 146183,
  • ENSG00000155719,
  • OTOA

Genome feature

Region: gene ? Length: 98658  
Location: 16:21663968-21762625 Cyto location: 16p12.2|16p12.2

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1 Diseases

Gene (Hum OR Rat) --> Mouse Allele (Phenotype)

Gene --> Alleles and Disease (clinVar data)

Gene -> HPO annotation (Human Phenotype Ontology)

Mouse Gene --> Allele [Phenotype]


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57 SN Ps

4 Cross References

16 Data Sets

7 Homologues

0 Located Features

97 Rna Seq Results