Entity Details

Primary name DIAP3_HUMAN
Entity type UniProt
Source Source Link

Details

AccessionQ9NSV4
EntryNameDIAP3_HUMAN
FullNameProtein diaphanous homolog 3
TaxID9606
Evidenceevidence at protein level
Length1193
SequenceStatuscomplete
DateCreated2001-02-21
DateModified2021-06-02

Ontological Relatives

GenesDIAPH3

GO terms

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GOName
GO:0003779 actin binding
GO:0005634 nucleus
GO:0005737 cytoplasm
GO:0005829 cytosol
GO:0007010 cytoskeleton organization
GO:0030036 actin cytoskeleton organization
GO:0030041 actin filament polymerization
GO:0031267 small GTPase binding
GO:0045296 cadherin binding

Subcellular Location

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Subcellular Location
Cytoplasm
Nucleus

Domains

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DomainNameCategoryType
IPR010465 DRF autoregulatoryDomainDomain
IPR010472 Formin, FH3 domainDomainDomain
IPR010473 Formin, GTPase-binding domainDomainDomain
IPR011989 Armadillo-like helicalFamilyHomologous superfamily
IPR014767 Diaphanous autoregulatory (DAD) domainDomainDomain
IPR014768 Rho GTPase-binding/formin homology 3 (GBD/FH3) domainDomainDomain
IPR015425 Formin, FH2 domainDomainDomain
IPR016024 Armadillo-type foldFamilyHomologous superfamily
IPR027654 Formin, protein diaphanous homologue 3FamilyFamily
IPR042201 Formin, FH2 domain superfamilyFamilyHomologous superfamily

Diseases

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Disease IDSourceNameDescription
609129 OMIMAuditory neuropathy, autosomal dominant, 1 (AUNA1)A form of sensorineural hearing loss with absent or severely abnormal auditory brainstem response, in the presence of normal cochlear outer hair cell function and normal otoacoustic emissions. Auditory neuropathies result from a lesion in the area including the inner hair cells, connections between the inner hair cells and the cochlear branch of the auditory nerve, the auditory nerve itself and auditory pathways of the brainstem. The disease is caused by variants affecting the gene represented in this entry. A disease-causing mutation in the conserved 5'-UTR leads to increased protein expression.