TMEM168 (transmembrane protein 168)

2014-11-01  

Identity

HGNC
LOCATION
7q31.1
LOCUSID
ALIAS
-
FUSION GENES

Other Information

Locus ID:

NCBI: 64418
HGNC: 25826
Ensembl: ENSG00000146802

Variants:

dbSNP: 64418
ClinVar: 64418
TCGA: ENSG00000146802
COSMIC: TMEM168

RNA/Proteins

Gene IDTranscript IDUniprot
ENSG00000146802ENST00000312814Q9H0V1
ENSG00000146802ENST00000312814A0A024R716
ENSG00000146802ENST00000418785H7C268
ENSG00000146802ENST00000441474C9IZT1
ENSG00000146802ENST00000447395Q9H0V1
ENSG00000146802ENST00000449743C9JVE9
ENSG00000146802ENST00000454074Q9H0V1
ENSG00000146802ENST00000454074A0A024R716

Expression (GTEx)

0
5
10
15
20

Protein levels (Protein atlas)

Not detected
Low
Medium
High

References

Pubmed IDYearTitleCitations
340868982021Transmembrane protein 168 mutation reduces cardiomyocyte cell surface expression of Nav1.5 through αB-crystallin intracellular dynamics.1
340868982021Transmembrane protein 168 mutation reduces cardiomyocyte cell surface expression of Nav1.5 through αB-crystallin intracellular dynamics.1
321756482020Identification of transmembrane protein 168 mutation in familial Brugada syndrome.3
321756482020Identification of transmembrane protein 168 mutation in familial Brugada syndrome.3
309402902019Inhibition of Proliferation by Knockdown of Transmembrane (TMEM) 168 in Glioblastoma Cells via Suppression of Wnt/β-Catenin Pathway.10
309402902019Inhibition of Proliferation by Knockdown of Transmembrane (TMEM) 168 in Glioblastoma Cells via Suppression of Wnt/β-Catenin Pathway.10
192400612009Coeliac disease-associated risk variants in TNFAIP3 and REL implicate altered NF-kappaB signalling.94
192400612009Coeliac disease-associated risk variants in TNFAIP3 and REL implicate altered NF-kappaB signalling.94

Citation

Dessen P

TMEM168 (transmembrane protein 168)

Atlas Genet Cytogenet Oncol Haematol. 2014-11-01

Online version: http://atlasgeneticsoncology.org/gene/74830/tmem168-(transmembrane-protein-168)