COX7B | ENSG00000131174 | NCBI 1349

Details for: COX7B

Gene ID: 1349

Symbol: COX7B

Ensembl ID: ENSG00000131174

Description: cytochrome c oxidase subunit 7B

Associated with

Cellular responses to stimuli
(R-HSA-8953897)
Cellular responses to stress
(R-HSA-2262752)
Cellular response to chemical stress
(R-HSA-9711123)
Cytoprotection by hmox1
(R-HSA-9707564)
Gene expression (transcription)
(R-HSA-74160)
Generic transcription pathway
(R-HSA-212436)
Metabolism
(R-HSA-1430728)
Respiratory electron transport
(R-HSA-611105)
Respiratory electron transport, atp synthesis by chemiosmotic coupling, and heat production by uncoupling proteins.
(R-HSA-163200)
Rna polymerase ii transcription
(R-HSA-73857)
The citric acid (tca) cycle and respiratory electron transport
(R-HSA-1428517)
Tp53 regulates metabolic genes
(R-HSA-5628897)
Transcriptional regulation by tp53
(R-HSA-3700989)
Cellular respiration
(GO:0045333)
Central nervous system development
(GO:0007417)
Cytochrome-c oxidase activity
(GO:0004129)
Mitochondrial electron transport, cytochrome c to oxygen
(GO:0006123)
Mitochondrial inner membrane
(GO:0005743)
Mitochondrial membrane
(GO:0031966)
Mitochondrial respiratory chain complex iv
(GO:0005751)
Mitochondrion
(GO:0005739)
Protein binding
(GO:0005515)
Proton transmembrane transport
(GO:1902600)
Respiratory chain complex iv
(GO:0045277)

Other Information

Proteins

Cytochrome c oxidase subunit 7B, mitochondrial

Genular Protein ID: 3497148990

Symbol: COX7B_HUMAN

Name: Cytochrome c oxidase subunit 7B, mitochondrial

UniProtKB Accession Codes:

P24311 B2R4M3 Q6ICR1

Database IDs:

Citations:

PubMed ID: 8382530

Title: Isolation of a cDNA specifying subunit VIIb of human cytochrome c oxidase.

PubMed ID: 8382530

DOI: 10.1016/0167-4781(93)90301-s

PubMed ID: 14702039

Title: Complete sequencing and characterization of 21,243 full-length human cDNAs.

PubMed ID: 14702039

DOI: 10.1038/ng1285

PubMed ID: 15772651

Title: The DNA sequence of the human X chromosome.

PubMed ID: 15772651

DOI: 10.1038/nature03440

PubMed ID: 15489334

Title: The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC).

PubMed ID: 15489334

DOI: 10.1101/gr.2596504

PubMed ID: 1309697

Title: Subunits VIIa,b,c of human cytochrome c oxidase. Identification of both 'heart-type' and 'liver-type' isoforms of subunit VIIa in human heart.

PubMed ID: 1309697

DOI: 10.1111/j.1432-1033.1992.tb19847.x

PubMed ID: 23122588

Title: Mutations in COX7B cause microphthalmia with linear skin lesions, an unconventional mitochondrial disease.

PubMed ID: 23122588

DOI: 10.1016/j.ajhg.2012.09.016

PubMed ID: 28844695

Title: Architecture of human mitochondrial respiratory megacomplex I2III2IV2.

PubMed ID: 28844695

DOI: 10.1016/j.cell.2017.07.050

PubMed ID: 30030519

Title: Structure of the intact 14-subunit human cytochrome c oxidase.

PubMed ID: 30030519

DOI: 10.1038/s41422-018-0071-1

Sequence Information:

Length: 80
Mass: 9161
Checksum: 1EE75BD1AA253E59
Sequence:

MFPLVKSALN RLQVRSIQQT MARQSHQKRT PDFHDKYGNA VLASGATFCI VTWTYVATQV 
GIEWNLSPVG RVTPKEWRNQ

The gene details are incomplete or unavailable at the moment.

Database document:

This is a preview of the gene's schema. Only a few entries are kept for 'singleCellExpressions,' 'mRNAExpressions,' and other large data arrays for visualization purposes. You can zoom in with the mouse wheel for a closer view, and the text will adjust automatically if necessary. For the full schema, download it here.

Details for: COX7B

Associated with

Other Information

Isolation of a cDNA specifying subunit VIIb of human cytochrome c oxidase. PubMed ID: 8382530

Complete sequencing and characterization of 21,243 full-length human cDNAs. PubMed ID: 14702039

The DNA sequence of the human X chromosome. PubMed ID: 15772651

The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC). PubMed ID: 15489334

Subunits VIIa,b,c of human cytochrome c oxidase. Identification of both 'heart-type' and 'liver-type' isoforms of subunit VIIa in human heart. PubMed ID: 1309697

Mutations in COX7B cause microphthalmia with linear skin lesions, an unconventional mitochondrial disease. PubMed ID: 23122588

Architecture of human mitochondrial respiratory megacomplex I2III2IV2. PubMed ID: 28844695

Structure of the intact 14-subunit human cytochrome c oxidase. PubMed ID: 30030519