Otoancorin

(Redirected from OTOA)

Otoancorin is a protein found in the vertebrate inner ear, on the sensory epithelia where it connects to the gel matrix.[5]

OTOA
Identifiers
AliasesOTOA, CT108, DFNB22, otoancorin
External IDsOMIM: 607038; MGI: 2149209; HomoloGene: 71803; GeneCards: OTOA; OMA:OTOA - orthologs
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_001161683
NM_144672
NM_170664

NM_139310

RefSeq (protein)

NP_001155155
NP_653273
NP_733764

NP_647471

Location (UCSC)Chr 16: 21.66 – 21.76 MbChr 7: 120.68 – 120.76 Mb
PubMed search[3][4]
Wikidata
View/Edit HumanView/Edit Mouse

Otoancorin is found in the cochlea, utricule, saccule, and under the cupulae on the surface of apical dells in the sensory epithelia.[6]

In humans the gene that encodes otoancorin is called OTOA. It is on chromosome 16p12.2 and contains 28 exons. A recessive mutation in this gene called IVS12+2T>C results in deafness. The human protein has 1,153 amino acids.[6]

In the mouse, this protein has 1088 amino acids.[6] In mice otoancorin is needed to attach the tectorial membrane to the inner hair cells in the cochlea.[7]

References

edit
  1. ^ a b c GRCh38: Ensembl release 89: ENSG00000155719Ensembl, May 2017
  2. ^ a b c GRCm38: Ensembl release 89: ENSMUSG00000034990Ensembl, May 2017
  3. ^ "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  4. ^ "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  5. ^ Deans MR, Peterson JM, Wong GW (September 2010). "Mammalian Otolin: a multimeric glycoprotein specific to the inner ear that interacts with otoconial matrix protein Otoconin-90 and Cerebellin-1". PLOS ONE. 5 (9): e12765. Bibcode:2010PLoSO...512765D. doi:10.1371/journal.pone.0012765. PMC 2939893. PMID 20856818.
  6. ^ a b c Zwaenepoel I, Mustapha M, Leibovici M, Verpy E, Goodyear R, Liu XZ, et al. (April 2002). "Otoancorin, an inner ear protein restricted to the interface between the apical surface of sensory epithelia and their overlying acellular gels, is defective in autosomal recessive deafness DFNB22". Proceedings of the National Academy of Sciences of the United States of America. 99 (9): 6240–5. Bibcode:2002PNAS...99.6240Z. doi:10.1073/pnas.082515999. PMC 122933. PMID 11972037.
  7. ^ Weddell T, Legan PK, Lukashkina VA, Goodyear RJ, Welstead L, Petit C, et al. (2011). "Otoancorin Knockout Mice Reveal Inertia is the Force for Hearing". American Institute of Physics Conference Series. AIP Conference Proceedings. 1403 (1): 139–140. Bibcode:2011AIPC.1403..139W. doi:10.1063/1.3658074.