SLITRK6

GENE INFORMATION

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Gene name

SLITRK6 (HGNC Symbol)

Synonyms

FLJ22774

Description

SLIT and NTRK-like family, member 6 (HGNC Symbol)

Entrez gene summary

This gene encodes a member of the SLITRK protein family. Members of this family are integral membrane proteins that are characterized by two N-terminal leucine-rich repeat (LRR) domains and a C-terminal region that shares homology with trk neurotrophin receptors. This protein functions as a regulator of neurite outgrowth required for normal hearing and vision. Mutations in this gene are a cause of myopia and deafness. [provided by RefSeq, Dec 2014]

Chromosome

13

Cytoband

q31.1

Chromosome location (bp)

86366925 - 86373623

Protein evidence

Evidence at protein level (all genes)

Ensembl

ENSG00000184564 (version 75.37)

Entrez gene

84189

UniProt

Q9H5Y7 (UniProt - Evidence at transcript level)

neXtProt

NX_Q9H5Y7

Antibodypedia

SLITRK6 antibodies
 

PROTEIN VIEW

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SLITRK6-001
 
 
 
 
 

PROTEIN INFORMATION

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Splice variant

Ensembl

UniProt

Protein class

Gene ontology

Length
(aa)

Molecular mass
(kDa)

Signal peptide
(predicted)

Transmembrane regions
(predicted)

SLITRK6-001 ENSP00000383143
ENST00000400286
Q9H5Y7
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