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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 7.0.0)

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,
  • MGI:2146199,
  • AW124904,
  • 2010309E21Rik,
  • Fam136a,
  • family with sequence similarity 136, member A,
  • RIKEN cDNA 2010309E21 gene

Features --> Cross References

Genome

Sequence Feature Displayer

JG Browse Displayer

0 Canonical

0 CDSs

0 Exons

0 Genomic Clusters

1 Involved In Mutations

0 Strain

0 Transcripts

0 Transgenic Expressors

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

Gene --> Proteins

Function

Mouse features --> Functions (GO terms)

Homology

Genes --> Homologs

Interactions

0 Pathways

0 Targeted By

Gene --> Protein-Protein Interactions

Expression

Gene --> Expression annotations

Phenotype

Genes/Features --> Phenotypes (MP terms)

Disease

Mouse features --> Human diseases

Literature

Mouse features --> Publications

 

Other

0 Driver For