Entity Details

Primary name SLITRK6
Entity type gene
Source Source Link

Details

PrimaryID84189
RefseqGeneNG_041801
SymbolSLITRK6
NameSLIT and NTRK like family member 6
Chromosome13
Location13q31.1
TaxID9606
Statuslive
SourceGenomegenomic
SourceOriginnatural
CreationDate2001-05-17
ModificationDate2021-06-11

Ontological Relatives

UniProt IDsSLIK6_HUMAN

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

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

3 interactions

InteractorPartnerSourcesPublicationsLink
SLITRK6CDC37IntAct25036637 details
SLITRK6H2BC5BioGRID, IntAct30021884 details
SLITRK6HRASBioGRID30639242 details