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Protein Coding Gene : Atpsckmt ATP synthase C subunit lysine N-methyltransferase

Primary Identifier  MGI:1915323 Organism  mouse, laboratory
Chromosome  15 NCBI Gene Number  68073
Mgi Type  protein coding gene
description  FUNCTION: Automated description from the Alliance of Genome Resources (Release 7.1.0)

Enables protein-lysine N-methyltransferase activity. Involved in positive regulation of sensory perception of pain and regulation of mitochondrial ATP synthesis coupled proton transport. Predicted to be located in mitochondrial crista. Predicted to be active in mitochondrion. Is expressed in embryo. Orthologous to human ATPSCKMT (ATP synthase c subunit lysine N-methyltransferase).
PHENOTYPE: Following carrageenan-induced priming, mice heterozygous for a null allele show a reduction in the magnitude of persistent prostaglandin E2-induced mechanical and thermal hyperalgesia. [provided by MGI curators]
  • synonyms:
  • expressed sequence AA987072,
  • Atpsckmt,
  • RIKEN cDNA A930016P21 gene,
  • Fam173b,
  • MGI:2145938,
  • A930016P21Rik,
  • ATP synthase C subunit lysine N-methyltransferase,
  • family with sequence similarity 173, member B,
  • AA987072

Features --> Cross References

Genome

Sequence Feature Displayer

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0 Canonical

0 CDSs

0 Exons

0 Genomic Clusters

2 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