COX6A1 (cytochrome c oxidase subunit 6A1)

2014-11-01  

Identity

HGNC
LOCATION
12q24.31
LOCUSID
ALIAS
CMTRID,COX6A,COX6AL
FUSION GENES

Other Information

Locus ID:

NCBI: 1337
MIM: 602072
HGNC: 2277
Ensembl: ENSG00000111775

Variants:

dbSNP: 1337
ClinVar: 1337
TCGA: ENSG00000111775
COSMIC: COX6A1

RNA/Proteins

Gene IDTranscript IDUniprot
ENSG00000111775ENST00000229379P12074
ENSG00000111775ENST00000229379H6SG15

Expression (GTEx)

0
100
200
300
400
500
600
700
800

Pathways

PathwaySourceExternal ID
Oxidative phosphorylationKEGGko00190
Alzheimer's diseaseKEGGko05010
Huntington's diseaseKEGGko05016
Oxidative phosphorylationKEGGhsa00190
Alzheimer's diseaseKEGGhsa05010
Parkinson's diseaseKEGGhsa05012
Huntington's diseaseKEGGhsa05016
Cardiac muscle contractionKEGGhsa04260
Cardiac muscle contractionKEGGko04260
Metabolic pathwaysKEGGhsa01100
Cytochrome c oxidaseKEGGhsa_M00154
Cytochrome c oxidaseKEGGM00154
Non-alcoholic fatty liver disease (NAFLD)KEGGhsa04932
Non-alcoholic fatty liver disease (NAFLD)KEGGko04932
Gene ExpressionREACTOMER-HSA-74160
Generic Transcription PathwayREACTOMER-HSA-212436
Transcriptional Regulation by TP53REACTOMER-HSA-3700989
TP53 Regulates Metabolic GenesREACTOMER-HSA-5628897
MetabolismREACTOMER-HSA-1430728
The citric acid (TCA) cycle and respiratory electron transportREACTOMER-HSA-1428517
Respiratory electron transport, ATP synthesis by chemiosmotic coupling, and heat production by uncoupling proteins.REACTOMER-HSA-163200
Respiratory electron transportREACTOMER-HSA-611105

Protein levels (Protein atlas)

Not detected
Low
Medium
High

References

Pubmed IDYearTitleCitations
256665582015Investigating the role of the physiological isoform switch of cytochrome c oxidase subunits in reversible mitochondrial disease.7
256665582015Investigating the role of the physiological isoform switch of cytochrome c oxidase subunits in reversible mitochondrial disease.7
251524552014A mutation of COX6A1 causes a recessive axonal or mixed form of Charcot-Marie-Tooth disease.37
251524552014A mutation of COX6A1 causes a recessive axonal or mixed form of Charcot-Marie-Tooth disease.37
203072582010Novel insights into the assembly and function of human nuclear-encoded cytochrome c oxidase subunits 4, 5a, 6a, 7a and 7b.44
208776242010Genetic variants in nuclear-encoded mitochondrial genes influence AIDS progression.20
203072582010Novel insights into the assembly and function of human nuclear-encoded cytochrome c oxidase subunits 4, 5a, 6a, 7a and 7b.44
208776242010Genetic variants in nuclear-encoded mitochondrial genes influence AIDS progression.20
198431592009Assembly of nuclear DNA-encoded subunits into mitochondrial complex IV, and their preferential integration into supercomplex forms in patient mitochondria.47
198431592009Assembly of nuclear DNA-encoded subunits into mitochondrial complex IV, and their preferential integration into supercomplex forms in patient mitochondria.47
185498092008Identification of cytochrome c oxidase subunit 6A1 as a suppressor of Bax-induced cell death by yeast-based functional screening.12
185498092008Identification of cytochrome c oxidase subunit 6A1 as a suppressor of Bax-induced cell death by yeast-based functional screening.12

Citation

Dessen P

COX6A1 (cytochrome c oxidase subunit 6A1)

Atlas Genet Cytogenet Oncol Haematol. 2014-11-01

Online version: http://atlasgeneticsoncology.org/gene/62041/gene-fusions-explorer/js/lib/favicon/apple-touch-icon.png