COX7B Gene Summary [Human]

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 subunit VIIb, which is highly similar to bovine COX VIIb protein and is found in all tissues. This gene may have several pseudogenes on chromosomes 1, 2, 20 and 22. [provided by RefSeq, Jun 2011]

Details

Type
Protein Coding
Official Symbol
COX7B
Official Name
cytochrome c oxidase subunit 7B [Source:HGNC Symbol;Acc:HGNC:2291]
Ensembl ID
ENSG00000131174
Bio databases IDs NCBI: 1349 Ensembl: ENSG00000131174
Aliases cytochrome c oxidase subunit 7B
Synonyms 1110004F07Rik, APLCC, cytochrome c oxidase subunit 7B, LSDMCA2
Species
Human, Homo sapiens
OrthologiesMouseRat

Protein Domains

A protein domain is a distinct structural or functional region within a protein that can evolve, function, and exist independently of the rest of the protein chain. These domains in human COX7B often fold into stable, three-dimensional structures and are associated with specific biological functions, such as binding to DNA, other proteins, or small molecules.
  • cytochrome-c oxidase
  • enzyme
  • protein binding
  • Cyt_c_Oxidase_VIIb

Pathways

Biological processes and signaling networks where the COX7B gene in human plays a role, providing insight into its function and relevance in health or disease.

Top Findings

The most significant associations for this gene, including commonly observed domains, pathway involvement, and functional highlights based on current data.
disease
  • reticulolinear aplasia cutis congenita with microcephaly, facial dysmorphism, and other congenital anomalies
  • metabolic syndrome X
  • Turner syndrome
  • Huntington disease
  • chronic obstructive pulmonary disease
  • insulin resistance
regulated by

Subcellular Expression

Locations within the cell where the protein is known or predicted to be active, providing insight into its function and cellular context.
  • Cytoplasm
  • Mitochondria
  • mitochondrial membrane
  • mitochondrial inner membrane

Gene Ontology Annotations

Describes the biological processes, cellular components, and molecular functions associated with the human COX7B gene, providing context for its role in the cell.

Biological Process

Functions and activities the gene product is involved in
  • central nervous system development
  • mitochondrial electron transport, cytochrome c to oxygen
  • cellular respiration

Cellular Component

Where in the cell the gene product is active
  • mitochondrial membrane
  • respiratory chain complex IV
  • mitochondrion
  • mitochondrial respiratory chain complex IV
  • mitochondrial inner membrane

Molecular Function

What the gene product does at the molecular level
  • protein binding
  • cytochrome-c oxidase activity

Gene-Specific Assays for Results You Can Trust

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