TMEM132E (transmembrane protein 132E)

2014-11-01  

Identity

HGNC
LOCATION
17q12
LOCUSID
ALIAS
DFNB99
FUSION GENES

Other Information

Locus ID:

NCBI: 124842
MIM: 616178
HGNC: 26991
Ensembl: ENSG00000181291

Variants:

dbSNP: 124842
ClinVar: 124842
TCGA: ENSG00000181291
COSMIC: TMEM132E

RNA/Proteins

Gene IDTranscript IDUniprot
ENSG00000181291ENST00000321639A0A494BWY4
ENSG00000181291ENST00000631683Q6IEE7

Expression (GTEx)

0
5
10
15
20
25
30
35

Protein levels (Protein atlas)

Not detected
Low
Medium
High

References

Pubmed IDYearTitleCitations
316563132020Further evidence of involvement of TMEM132E in autosomal recessive nonsyndromic hearing impairment.7
329290052020Hair cell α9α10 nicotinic acetylcholine receptor functional expression regulated by ligand binding and deafness gene products.9
316563132020Further evidence of involvement of TMEM132E in autosomal recessive nonsyndromic hearing impairment.7
329290052020Hair cell α9α10 nicotinic acetylcholine receptor functional expression regulated by ligand binding and deafness gene products.9
253316382015Whole-exome sequencing identifies a variant in TMEM132E causing autosomal-recessive nonsyndromic hearing loss DFNB99.23
253316382015Whole-exome sequencing identifies a variant in TMEM132E causing autosomal-recessive nonsyndromic hearing loss DFNB99.23

Citation

Dessen P

TMEM132E (transmembrane protein 132E)

Atlas Genet Cytogenet Oncol Haematol. 2014-11-01

Online version: http://atlasgeneticsoncology.org/gene/74796/gene-fusions-explorer/js/meetings/