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Protein Coding Gene : Plekhn1 pleckstrin homology domain containing, family N member 1

Primary Identifier  MGI:2387630 Organism  mouse, laboratory
Chromosome  4 NCBI Gene Number  231002
Mgi Type  protein coding gene
description  FUNCTION: Automated description from the Alliance of Genome Resources (Release 8.0.0)

Predicted to enable phospholipid binding activity. Involved in 3'-UTR-mediated mRNA destabilization. Located in mitochondrion. Orthologous to human PLEKHN1 (pleckstrin homology domain containing N1).
PHENOTYPE: Older male mice homozygous for a knock-out allele develop obesity associated with increased epididymal fat pad and liver weight, hyperphagia and increased circulating leptin levels. [provided by MGI curators]
  • synonyms:
  • cDNA sequence BC025458,
  • pleckstrin homology domain containing, family N member 1,
  • Plekhn1,
  • BC025458

Features --> Cross References

Genome

Sequence Feature Displayer

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0 Canonical

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