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Protein Coding Gene : Atp5f1d ATP synthase F1 subunit delta
Primary Identifier  MGI:1913293 Organism  mouse, laboratory
Chromosome  10 NCBI Gene Number  66043
Mgi Type  protein coding gene
description  FUNCTION: Automated description from the Alliance of Genome Resources (Release 7.1.0)

Predicted to enable proton transmembrane transporter activity. Predicted to contribute to ATP hydrolysis activity and proton-transporting ATP synthase activity, rotational mechanism. Predicted to be involved in mitochondrial proton-transporting ATP synthase complex assembly and proton motive force-driven mitochondrial ATP synthesis. Predicted to act upstream of or within proton transmembrane transport. Located in mitochondrial inner membrane. Is expressed in several structures, including alimentary system; eye; genitourinary system; integumental system; and nervous system. Human ortholog(s) of this gene implicated in mitochondrial complex V (ATP synthase) deficiency nuclear type 5. Orthologous to human ATP5F1D (ATP synthase F1 subunit delta).
  • synonyms:
  • expressed sequence C85518,
  • AU020773,
  • MGI:1924154,
  • ATP synthase, H+ transporting, mitochondrial F1 complex, delta subunit,
  • ATP synthase, H+ transporting, mitochondrial F1 complex, delta subunit,
  • MGI:2143942,
  • 0610008F14Rik,
  • MGI:2143703,
  • expressed sequence AI876556,
  • C85518,
  • MGI:2143512,
  • Atp5d,
  • MGI:2143772,
  • RIKEN cDNA 0610008F14 gene,
  • expressed sequence AU020773,
  • AA960090,
  • AI876556,
  • ATP synthase F1 subunit delta,
  • expressed sequence AA960090,
  • RIKEN cDNA 1500000I11 gene,
  • Atp5f1d,
  • 1500000I11Rik
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Genome

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1 Involved In Mutations

Trail: ProteinCodingGene

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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

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Function

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Homology

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Interactions

7 Pathways

Trail: ProteinCodingGene

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Gene --> Protein-Protein Interactions

Expression

Gene --> Expression annotations

Phenotype

Genes/Features --> Phenotypes (MP terms)

Disease

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