COX17

GENERAL INFORMATION

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Gene name

COX17

Gene description

COX17 cytochrome c oxidase copper chaperone

Protein class

Cancer-related genes
Mitochondrial proteins
Predicted intracellular proteins

Predicted localization

Intracellular

Number of transcripts

3
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HUMAN PROTEIN ATLAS INFORMATION

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RNA tissue category

HPA:Expressed in all
GTEx:Expressed in all

Protein evidence

Evidence at protein level

Protein localization

General granular cytoplasmic expression.

ANTIBODY RELIABILITY

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Data reliability
description

Pending RNA-based expert annotation.

Data reliability

Supportive based on 2 antibodies.
HPA042226 , HPA048158
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RNA AND PROTEIN EXPRESSION SUMMARY

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RNA expression (FPKM) Protein expression (score)
Brain
Endocrine tissues
Bone marrow & immune system
Muscle tissues
Lung
Liver & gallbladder
Pancreas
Gastrointestinal tract
Kidney & urinary bladder
Male tissues
Female tissues
Adipose & soft tissue
Skin
Cerebral cortex

Lymph node

Liver

Colon

Kidney

Testis



PROTEIN EXPRESSION OVERVIEW

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Organ

Expression



RNA EXPRESSION OVERVIEW

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HPA dataset
RNA tissue category:  Expressed in all

Organ

Expression

GTEx dataset
RNA tissue category:  Expressed in all

Organ

Expression



GENE INFORMATION

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Gene name

COX17

Synonyms

Description

COX17 cytochrome c oxidase copper chaperone (HGNC Symbol)

Entrez gene summary

Cytochrome c oxidase (COX), the terminal component of the mitochondrial respiratory chain, catalyzes the electron transfer from reduced cytochrome c to oxygen. This component is a heteromeric complex consisting of 3 catalytic subunits encoded by mitochondrial genes and multiple structural subunits encoded by nuclear genes. The mitochondrially-encoded subunits function in electron transfer, and the nuclear-encoded subunits may function in the regulation and assembly of the complex. This nuclear gene encodes a protein which is not a structural subunit, but may be involved in the recruitment of copper to mitochondria for incorporation into the COX apoenzyme. This protein shares 92% amino acid sequence identity with mouse and rat Cox17 proteins. This gene is no longer considered to be a candidate gene for COX deficiency. A pseudogene COX17P has been found on chromosome 13. [provided by RefSeq, Jul 2008]

Chromosome

3

Cytoband

q13.33

Chromosome location (bp)

119654513 - 119677454

Protein evidence

Evidence at protein level (all genes)

Ensembl

ENSG00000138495 (version 78.38)

Entrez gene

10063

UniProt

Q14061 (UniProt - Evidence at protein level)

neXtProt

NX_Q14061

Antibodypedia

COX17 antibodies


PROTEIN BROWSER

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ENST00000261070
 
ENST00000484810
 
ENST00000497116
 
 
 
 


PROTEIN INFORMATION

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Splice variant

Ensembl

UniProt

Protein class

Gene ontology

Length
(aa)

Molecular mass
(kDa)

Signal peptide
(predicted)

Transmembrane regions
(predicted)

COX17-001 ENSP00000261070
ENST00000261070
Q14061
Show all »
Show » Show » 63 6.9 No 0
COX17-005 ENSP00000417651
ENST00000484810
C9J8T6
Show all »
Show » Show » 98 10.9 No 0
COX17-006 ENSP00000417923
ENST00000497116
Q14061
Show all »
Show » Show » 63 6.9 No 0