Ndufa1 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 alimentary system; central nervous system; cranium; respiratory system; and sensory organ. Used to study mitochondrial complex I deficiency. Human ortholog(s) of this gene implicated in nuclear type mitochondrial complex I deficiency 12. Orthologous to human NDUFA1 (NADH:ubiquinone oxidoreductase subunit A1). [provided by Alliance of Genome Resources, Apr 2025]

Details

Type
Protein Coding
Official Symbol
Ndufa1
Official Name
NADH:ubiquinone oxidoreductase subunit A1 [Source:MGI Symbol;Acc:MGI:1929511]
Ensembl ID
ENSMUSG00000016427
Bio databases IDs NCBI: 54405 Ensembl: ENSMUSG00000016427
Aliases NADH:ubiquinone oxidoreductase subunit A1
Synonyms 1810049F12Rik, CI-MWFE, Complex I-MWFE, LOC108348144, MC1DN12, MWFE, NADH ubiquinone Oxidoreductase MWFE subunit, NADH:ubiquinone oxidoreductase subunit A1, RGD1560955, ZNF183
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 Ndufa1 often fold into stable, three-dimensional structures and are associated with specific biological functions, such as binding to DNA, other proteins, or small molecules.
  • NADH-ubiquinone oxidoreductase MWFE subunit
  • NADH2 dehydrogenase
  • enzyme
  • NADH2 dehydrogenase (ubiquinone)

Pathways

Biological processes and signaling networks where the Ndufa1 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
  • hereditary disorder
  • chronic kidney disease
  • Huntington disease
  • septic shock
  • nuclear type 12 mitochondrial complex I deficiency
  • Leigh syndrome
  • adult acute myeloid leukemia
regulated by
role in cell
  • survival
  • morphology

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 mouse Ndufa1 gene, providing context for its role in the cell.

Biological Process

Functions and activities the gene product is involved in
  • transmembrane transport
  • mitochondrial electron transport, NADH to ubiquinone
  • 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
  • mitochondrial membrane
  • mitochondrion
  • mitochondrial inner membrane

Molecular Function

What the gene product does at the molecular level
  • NADH dehydrogenase (ubiquinone) activity

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.