Entity Details

Primary name TPRN_HUMAN
Entity type UniProt
Source Source Link

Details

AccessionQ4KMQ1
EntryNameTPRN_HUMAN
FullNameTaperin
TaxID9606
Evidenceevidence at protein level
Length711
SequenceStatuscomplete
DateCreated2008-04-29
DateModified2021-06-02

Ontological Relatives

GenesTPRN

GO terms

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GOName
GO:0007605 sensory perception of sound
GO:0019902 phosphatase binding
GO:0032420 stereocilium
GO:0060088 auditory receptor cell stereocilium organization
GO:0120044 stereocilium base
GO:0120045 stereocilium maintenance

Subcellular Location

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Subcellular Location
Cell projection

Domains

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DomainNameCategoryType
IPR025903 Phostensin/Taperin N-terminal domainDomainDomain
IPR025907 Phostensin/Taperin PP1-binding domainDomainDomain
IPR026671 Phostensin/TaperinFamilyFamily
IPR033359 TaperinFamilyFamily

Diseases

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Disease IDSourceNameDescription
613307 OMIMDeafness, autosomal recessive, 79 (DFNB79)A form of non-syndromic deafness characterized by progressive and severe sensorineural hearing loss. There are no symptoms of vestibular dysfunction. The disease is caused by variants affecting the gene represented in this entry.