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Protein Coding Gene : Mss51 MSS51 mitochondrial translational activator

Primary Identifier  MGI:1922093 Organism  mouse, laboratory
Chromosome  14 NCBI Gene Number  74843
Mgi Type  protein coding gene
description  FUNCTION: Automated description from the Alliance of Genome Resources (Release 7.0.0)

Predicted to enable metal ion binding activity. Orthologous to human MSS51 (MSS51 mitochondrial translational activator).
PHENOTYPE: Mice homozygous for a null allele exhibit glucose intolerance, insulin resistance, and hepatic steatosis when fed a high-fat diet. Muscle shows mitochondrial abnormalities and mice show decreased running performance. [provided by MGI curators]
  • synonyms:
  • zinc finger, MYND domain containing 17,
  • RIKEN cDNA 4833444M15 gene,
  • MSS51 mitochondrial translational activator,
  • Mss51,
  • Zmynd17,
  • 4833444M15Rik

Features --> Cross References

Genome

Sequence Feature Displayer

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0 CDSs

0 Exons

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0 Involved In Mutations

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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

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Gene --> Protein-Protein Interactions

Expression

Gene --> Expression annotations

Phenotype

Genes/Features --> Phenotypes (MP terms)

Disease

Mouse features --> Human diseases

Literature

Mouse features --> Publications

 

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0 Driver For