Ndufb11 Gene Summary [Mouse]

Predicted to be involved in mitochondrial respiratory chain complex I assembly. Located in mitochondrion. Part of respiratory chain complex I. Is active in mitochondrial inner membrane. Is expressed in several structures, including central nervous system; genitourinary system; hemolymphoid system gland; sensory organ; and trunk mesenchyme. Human ortholog(s) of this gene implicated in linear skin defects with multiple congenital anomalies 3 and nuclear type mitochondrial complex I deficiency 30. Orthologous to human NDUFB11 (NADH:ubiquinone oxidoreductase subunit B11). [provided by Alliance of Genome Resources, Apr 2025]

Details

Type
Protein Coding
Official Symbol
Ndufb11
Official Name
NADH:ubiquinone oxidoreductase subunit B11 [Source:MGI Symbol;Acc:MGI:1349919]
Ensembl ID
ENSMUSG00000031059
Bio databases IDs NCBI: 104130 Ensembl: ENSMUSG00000031059
Aliases NADH:ubiquinone oxidoreductase subunit B11
Synonyms CI-ESSS, D5Bwg0566e, D5Bwg0577e, ESSS, MC1DN30, NADH:ubiquinone oxidoreductase subunit B11, Neuronal protein 15.6, Np15, NP15.6, NP17.3, p15.6, P17.3, RGD1563698
Species
Mouse, Mus musculus
OrthologiesHumanRat

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 mouse Ndufb11 often fold into stable, three-dimensional structures and are associated with specific biological functions, such as binding to DNA, other proteins, or small molecules.
  • enzyme
  • protein binding
  • ESSS subunit of NADH:ubiquinone oxidoreductase (complex I)

Pathways

Biological processes and signaling networks where the Ndufb11 gene in mouse 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
  • mitochondrial disorder
  • linear skin defects with multiple congenital anomalies 3
  • hereditary sideroblastic anemia
  • neurodevelopmental disorder
  • nuclear type 30 mitochondrial complex I deficiency
  • respiratory insufficiency
  • infantile histiocytoid cardiomyopathy
  • insulin resistance
regulated by
regulates
  • Mitochondrial ETC 1
role in cell
  • proliferation

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
  • pH resistant lipid raft fraction
  • Mitochondria
  • mitochondrial inner membrane

Gene Ontology Annotations

Describes the biological processes, cellular components, and molecular functions associated with the mouse Ndufb11 gene, providing context for its role in the cell.

Biological Process

Functions and activities the gene product is involved in
  • mitochondrial respiratory chain complex I assembly
  • aerobic respiration
  • mitochondrial ATP synthesis coupled proton transport

Cellular Component

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

Molecular Function

What the gene product does at the molecular level
  • protein binding

Gene-Specific Assays for Results You Can Trust

Streamline your workflow with assays designed for this gene. Our targeted dPCR and qPCR assays help you generate meaningful data – efficiently and accurately.