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Protein Coding Gene : Atp5f1e ATP synthase F1 subunit epsilon
Primary Identifier  MGI:1855697 Organism  mouse, laboratory
Chromosome  2 NCBI Gene Number  67126
Mgi Type  protein coding gene
description  FUNCTION: Automated description from the Alliance of Genome Resources (Release 7.0.0)

Predicted to enable P-type proton-exporting transporter activity. Predicted to contribute to ATP hydrolysis activity and proton-transporting ATP synthase activity, rotational mechanism. Predicted to be involved in proton motive force-driven mitochondrial ATP synthesis. Predicted to act upstream of or within proton motive force-driven ATP synthesis. Located in mitochondrial inner membrane. Human ortholog(s) of this gene implicated in mitochondrial complex V (ATP synthase) deficiency nuclear type 3. Orthologous to several human genes including ATP5F1E (ATP synthase F1 subunit epsilon).
  • synonyms:
  • Atp5f1e,
  • Atp5e,
  • 2410043G19Rik,
  • MGI:1914376,
  • expressed sequence AV000645,
  • ATP synthase F1 subunit epsilon,
  • MGI:2139226,
  • AV000645,
  • RIKEN cDNA 2410043G19 gene,
  • ATP synthase, H+ transporting, mitochondrial F1 complex, epsilon subunit
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Features --> Cross References

Genome

Sequence Feature Displayer

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0 CDSs

0 Exons

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0 Involved In Mutations

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0 Transgenic Expressors

0 UTRs

Canonical gene --> CDSs in specific strains.

Canonical gene --> Exons in specific strains

Canonical gene --> Strain-specific IDs, biotypes, and locations

Canonical gene --> Transcripts in specific strains.

Features --> Overlapping features

Proteins

Gene --> Proteins

Function

Mouse features --> Functions (GO terms)

Homology

Genes --> Homologs

Interactions

7 Pathways

0 Targeted By

Gene --> Protein-Protein Interactions

Expression

Gene --> Expression annotations

Phenotype

Genes/Features --> Phenotypes (MP terms)

Disease

Mouse features --> Human diseases

Literature

Mouse features --> Publications

 

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