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Protein Coding Gene : Ptdss2 phosphatidylserine synthase 2
Primary Identifier  MGI:1351664 Organism  mouse, laboratory
Chromosome  7 NCBI Gene Number  27388
Mgi Type  protein coding gene
description  FUNCTION: Automated description from the Alliance of Genome Resources (Release 7.1.0)

Enables CDP-diacylglycerol-serine O-phosphatidyltransferase activity and L-serine-phosphatidylethanolamine phosphatidyltransferase activity. Acts upstream of or within phosphatidylserine biosynthetic process. Located in endoplasmic reticulum membrane. Is expressed in several structures, including genitourinary system; hemolymphoid system; liver; lung; and nervous system. Orthologous to human PTDSS2 (phosphatidylserine synthase 2).
PHENOTYPE: Disruption of this gene causes infertility in about 10% of homozygous males. The remaining males and all females were fertile. [provided by MGI curators]
  • synonyms:
  • Ptdss2,
  • expressed sequence AI481134,
  • MGI:2141985,
  • AI988017,
  • AI481134,
  • phosphatidylserine synthase 2,
  • PSS2,
  • expressed sequence AI988017,
  • MGI:2142082
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Features --> Cross References

Genome

Sequence Feature Displayer

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0 Canonical

0 CDSs

0 Exons

0 Genomic Clusters

1 Involved In Mutations

Trail: ProteinCodingGene

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

5 Pathways

Trail: ProteinCodingGene

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

 

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0 Driver For





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