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Protein Coding Gene : Slc25a26 solute carrier family 25 (mitochondrial carrier, phosphate carrier), member 26
Primary Identifier  MGI:1914832 Organism  mouse, laboratory
Chromosome  6 NCBI Gene Number  67582
Mgi Type  protein coding gene
description  FUNCTION: Automated description from the Alliance of Genome Resources (Release 7.1.0)

Predicted to enable S-adenosyl-L-methionine:S-adenosyl-L-homocysteine antiporter activity. Predicted to be involved in mitochondrial S-adenosyl-L-methionine transmembrane transport. Located in mitochondrion. Human ortholog(s) of this gene implicated in combined oxidative phosphorylation deficiency 28. Orthologous to human SLC25A26 (solute carrier family 25 member 26).
PHENOTYPE: Embryos homozygous for a transposon insertion appear growth retarded and underdeveloped and die after E8.5 but prior to birth. [provided by MGI curators]
  • synonyms:
  • RIKEN cDNA 4933433F13 gene,
  • D6Bwg0781e,
  • MGD-MRK-34162,
  • MGI:2141709,
  • DNA segment, Chr 6, Brigham & Women's Genetics 0781 expressed,
  • solute carrier family 25 (mitochondrial carrier, phosphate carrier), member 26,
  • RIKEN cDNA 4930433D19 gene,
  • expressed sequence AW557176,
  • 4933433F13Rik,
  • 4930433D19Rik,
  • MGI:106468,
  • Slc25a26,
  • MGI:1918503,
  • AW557176
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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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Interactions

3 Pathways

Trail: ProteinCodingGene

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Gene --> Protein-Protein Interactions

Expression

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Phenotype

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Mouse features --> Human diseases

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