Entity Details

Primary name SLIK6_HUMAN
Entity type UniProt
Source Source Link

Details

AccessionQ9H5Y7
EntryNameSLIK6_HUMAN
FullNameSLIT and NTRK-like protein 6
TaxID9606
Evidenceevidence at transcript level
Length841
SequenceStatuscomplete
DateCreated2004-04-13
DateModified2021-06-02

Ontological Relatives

GenesSLITRK6

GO terms

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GOName
GO:0001964 startle response
GO:0002088 lens development in camera-type eye
GO:0002093 auditory receptor cell morphogenesis
GO:0005886 plasma membrane
GO:0005887 integral component of plasma membrane
GO:0007409 axonogenesis
GO:0007416 synapse assembly
GO:0007601 visual perception
GO:0007605 sensory perception of sound
GO:0008344 adult locomotory behavior
GO:0009986 cell surface
GO:0021562 vestibulocochlear nerve development
GO:0031223 auditory behavior
GO:0035264 multicellular organism growth
GO:0051965 positive regulation of synapse assembly
GO:0060007 linear vestibuloocular reflex
GO:0060384 innervation
GO:0090102 cochlea development
GO:1905606 regulation of presynapse assembly

Subcellular Location

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Subcellular Location
Cell membrane

Domains

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DomainNameCategoryType
IPR000483 Cysteine-rich flanking region, C-terminalDomainDomain
IPR001611 Leucine-rich repeatRepeatRepeat
IPR003591 Leucine-rich repeat, typical subtypeRepeatRepeat
IPR032675 Leucine-rich repeat domain superfamilyFamilyHomologous superfamily
IPR043326 Slitrk familyFamilyFamily

Diseases

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Disease IDSourceNameDescription
221200 OMIMDeafness and myopia (DFNMYP)An autosomal recessive disorder characterized by prelingual sensorineural hearing loss associated with high myopia. The disease is caused by variants affecting the gene represented in this entry.

Interactions

1 interaction

InteractorPartnerSourcesPublicationsLink
SLIK6_HUMANCDC37_HUMANIntAct25036637 details