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Protein Coding Gene : Sppl3 signal peptide peptidase 3

Primary Identifier  MGI:1891433 Organism  mouse, laboratory
Chromosome  5 NCBI Gene Number  74585
Mgi Type  protein coding gene
description  FUNCTION: Automated description from the Alliance of Genome Resources (Release 7.0.0)

Predicted to enable aspartic endopeptidase activity, intramembrane cleaving and protein homodimerization activity. Involved in T cell receptor signaling pathway; positive regulation of calcineurin-NFAT signaling cascade; and positive regulation of cytosolic calcium ion concentration. Located in endoplasmic reticulum-Golgi intermediate compartment membrane. Is expressed in central nervous system; gonad; retina; and vibrissa. Orthologous to human SPPL3 (signal peptide peptidase like 3).
PHENOTYPE: Mice homozygous for a gene trap insertion exhibit growth retardation, reduced fertility and behavioral abnormalities. Mice homozygous for a constitutive null allele or a protease-dead allele show neonatal and postnatal lethality. [provided by MGI curators]
  • synonyms:
  • MGI:1921835,
  • RIKEN cDNA 4833416I09 gene,
  • signal peptide peptidase 3,
  • Usmg3,
  • Sppl3,
  • 4833416I09Rik,
  • upregulated during skeletal muscle growth 3

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

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0 Driver For