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Protein Coding Gene : mt-Nd5 mitochondrially encoded NADH dehydrogenase 5
Primary Identifier  MGI:102496 Organism  mouse, laboratory
Chromosome  MT NCBI Gene Number  17721
Mgi Type  protein coding gene
description  FUNCTION: Automated description from the Alliance of Genome Resources (Release 7.1.0)

Contributes to NADH dehydrogenase (ubiquinone) activity. Predicted to be involved in electron transport coupled proton transport; mitochondrial electron transport, NADH to ubiquinone; and mitochondrial respiratory chain complex I assembly. Located in mitochondrion. Is expressed in central nervous system; heart; liver; metanephros; and retina. Human ortholog(s) of this gene implicated in Leber hereditary optic neuropathy; Leigh disease; and MELAS syndrome. Orthologous to human MT-ND5 (mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 5).
  • synonyms:
  • AU018746,
  • expressed sequence AU018746,
  • MGI:2145346,
  • AU018713,
  • URF5,
  • expressed sequence AU018713,
  • MGI:2145345,
  • MGD-MRK-19333,
  • mt-Nd5,
  • MGI:1925612,
  • RIKEN cDNA 0610010I05 gene,
  • mitochondrially encoded NADH dehydrogenase 5,
  • 0610010I05Rik
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Features --> Cross References

Genome

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1 Involved In Mutations

Trail: ProteinCodingGene

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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

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Function

Mouse features --> Functions (GO terms)

Homology

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Interactions

5 Pathways

Trail: ProteinCodingGene

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Gene --> Protein-Protein Interactions

Expression

Gene --> Expression annotations

Phenotype

Genes/Features --> Phenotypes (MP terms)

Disease

Mouse features --> Human diseases

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