SLC7A14 (solute carrier family 7 member 14)

2014-11-01  

Identity

HGNC
LOCATION
3q26.2
LOCUSID
ALIAS
PPP1R142

Other Information

Locus ID:

NCBI: 57709
MIM: 615720
HGNC: 29326
Ensembl: ENSG00000013293

Variants:

dbSNP: 57709
ClinVar: 57709
TCGA: ENSG00000013293
COSMIC: SLC7A14

RNA/Proteins

Gene IDTranscript IDUniprot
ENSG00000013293ENST00000231706Q8TBB6

Expression (GTEx)

0
5
10
15
20
25

Protein levels (Protein atlas)

Not detected
Low
Medium
High

References

Pubmed IDYearTitleCitations
203796142010Personalized smoking cessation: interactions between nicotine dose, dependence and quit-success genotype score.62
246708722014SLC7A14 linked to autosomal recessive retinitis pigmentosa.26
227871432012A chimera carrying the functional domain of the orphan protein SLC7A14 in the backbone of SLC7A2 mediates trans-stimulated arginine transport.2
309243912019Phenotypic variability of SLC7A14 mutations in patients with inherited retinal dystrophy.1
270284802017Screening for SLC7A14 gene mutations in patients with autosomal recessive or sporadic retinitis pigmentosa.0

Citation

Dessen P

SLC7A14 (solute carrier family 7 member 14)

Atlas Genet Cytogenet Oncol Haematol. 2014-11-01

Online version: http://atlasgeneticsoncology.org/gene/73483/slc7a14