SLITRK6 (SLIT and NTRK like family member 6)

2014-11-01  

Identity

HGNC
LOCATION
13q31.1
LOCUSID
ALIAS
DFNMYP

Other Information

Locus ID:

NCBI: 84189
MIM: 609681
HGNC: 23503
Ensembl: ENSG00000184564

Variants:

dbSNP: 84189
ClinVar: 84189
TCGA: ENSG00000184564
COSMIC: SLITRK6

RNA/Proteins

Gene IDTranscript IDUniprot
ENSG00000184564ENST00000643778Q9H5Y7
ENSG00000184564ENST00000647374Q9H5Y7

Expression (GTEx)

0
5
10
15
20
25
30
35
40

Protein levels (Protein atlas)

Not detected
Low
Medium
High

References

Pubmed IDYearTitleCitations
235430542013SLITRK6 mutations cause myopia and deafness in humans and mice.16
239461382014A homozygous SLITRK6 nonsense mutation is associated with progressive auditory neuropathy in humans.0
275309372017Human cytomegalovirus downregulates SLITRK6 expression through IE2.0
295514972018A novel mutation in SLITRK6 causes deafness and myopia in a Moroccan family.0

Citation

Dessen P

SLITRK6 (SLIT and NTRK like family member 6)

Atlas Genet Cytogenet Oncol Haematol. 2014-11-01

Online version: http://atlasgeneticsoncology.org/gene/73524/slitrk6