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Protein Coding Gene : Slc25a20 solute carrier family 25 (mitochondrial carnitine/acylcarnitine translocase), member 20
Primary Identifier  MGI:1928738 Organism  mouse, laboratory
Chromosome  9 NCBI Gene Number  57279
Mgi Type  protein coding gene
description  FUNCTION: Automated description from the Alliance of Genome Resources (Release 7.1.0)

Predicted to enable acyl carnitine transmembrane transporter activity. Acts upstream of or within in utero embryonic development. Located in mitochondrial inner membrane. Is expressed in cerebral cortex ventricular layer and cortical plate. Human ortholog(s) of this gene implicated in carnitine-acylcarnitine translocase deficiency. Orthologous to human SLC25A20 (solute carrier family 25 member 20).
PHENOTYPE: Mice homozygous for a knock-out allele exhibit placenta hemorrhage and complete preweaning lethality. [provided by MGI curators]
  • synonyms:
  • Cact,
  • expressed sequence C78826,
  • C78826,
  • carnitine/acylcarnitine translocase,
  • Slc25a20,
  • MGI:2143399,
  • solute carrier family 25 (mitochondrial carnitine/acylcarnitine translocase), member 20,
  • 1110007P09Rik,
  • RIKEN cDNA 1110007P09 gene,
  • mCAC,
  • MGI:1919042
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