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Protein Coding Gene : Fam136a family with sequence similarity 136, member A
Primary Identifier  MGI:1913738 Organism  mouse, laboratory
Chromosome  6 NCBI Gene Number  66488
Mgi Type  protein coding gene
description  FUNCTION: Automated description from the Alliance of Genome Resources (Release 8.0.0)

Located in mitochondrion. Is expressed in several structures, including alimentary system; orbito-sphenoid; renal cortex; respiratory system; and submandibular gland primordium. Orthologous to human FAM136A (family with sequence similarity 136 member A).
PHENOTYPE: Mice homozygous for a knock-out allele exhibit increased susceptibility to age-related hearing loss . [provided by MGI curators]
  • synonyms:
  • expressed sequence AW124904,
  • 2010309E21Rik,
  • Fam136a,
  • AW124904,
  • MGI:2146199,
  • family with sequence similarity 136, member A,
  • RIKEN cDNA 2010309E21 gene
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1 Involved In Mutations

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Canonical gene --> CDSs in specific strains.

Canonical gene --> Exons in specific strains

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