TMEM126A (transmembrane protein 126A)

2014-11-01  

Identity

HGNC
LOCATION
11q14.1
LOCUSID
ALIAS
OPA7

Other Information

Locus ID:

NCBI: 84233
MIM: 612988
HGNC: 25382
Ensembl: ENSG00000171202

Variants:

dbSNP: 84233
ClinVar: 84233
TCGA: ENSG00000171202
COSMIC: TMEM126A

RNA/Proteins

Gene IDTranscript IDUniprot
ENSG00000171202ENST00000304511Q9H061
ENSG00000171202ENST00000525353E9PIH8
ENSG00000171202ENST00000528105Q9H061
ENSG00000171202ENST00000531366E9PI90
ENSG00000171202ENST00000532180Q9H061

Expression (GTEx)

0
10
20
30
40
50
60
70
80

Protein levels (Protein atlas)

Not detected
Low
Medium
High

References

Pubmed IDYearTitleCitations
338796112021Optic atrophy-associated TMEM126A is an assembly factor for the ND4-module of mitochondrial complex I.10
338823092021NDUFS3 depletion permits complex I maturation and reveals TMEM126A/OPA7 as an assembly factor binding the ND4-module intermediate.13
338796112021Optic atrophy-associated TMEM126A is an assembly factor for the ND4-module of mitochondrial complex I.10
338823092021NDUFS3 depletion permits complex I maturation and reveals TMEM126A/OPA7 as an assembly factor binding the ND4-module intermediate.13
303931592019Loss of TMEM126A promotes extracellular matrix remodeling, epithelial-to-mesenchymal transition, and breast cancer metastasis by regulating mitochondrial retrograde signaling.14
309615382019Novel likely pathogenic variants in TMEM126A identified in non-syndromic autosomal recessive optic atrophy: two case reports.6
303931592019Loss of TMEM126A promotes extracellular matrix remodeling, epithelial-to-mesenchymal transition, and breast cancer metastasis by regulating mitochondrial retrograde signaling.14
309615382019Novel likely pathogenic variants in TMEM126A identified in non-syndromic autosomal recessive optic atrophy: two case reports.6
235000702013TMEM126A is a mitochondrial located mRNA (MLR) protein of the mitochondrial inner membrane.12
235000702013TMEM126A is a mitochondrial located mRNA (MLR) protein of the mitochondrial inner membrane.12
228156382012TMEM126A mutation in a Moroccan family with autosomal recessive optic atrophy.9
228156382012TMEM126A mutation in a Moroccan family with autosomal recessive optic atrophy.9
204050262010Nonsense mutation in TMEM126A causing autosomal recessive optic atrophy and auditory neuropathy.21
208776242010Genetic variants in nuclear-encoded mitochondrial genes influence AIDS progression.20
204050262010Nonsense mutation in TMEM126A causing autosomal recessive optic atrophy and auditory neuropathy.21

Citation

Dessen P

TMEM126A (transmembrane protein 126A)

Atlas Genet Cytogenet Oncol Haematol. 2014-11-01

Online version: http://atlasgeneticsoncology.org/gene/74787/css/js/lib/hgnc