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Protein Coding Gene : Phospho1 phosphatase, orphan 1
Primary Identifier  MGI:2447348 Organism  mouse, laboratory
Chromosome  11 NCBI Gene Number  237928
Mgi Type  protein coding gene
description  FUNCTION: Automated description from the Alliance of Genome Resources (Release 8.0.0)

Predicted to enable phosphocholine phosphatase activity; phosphoethanolamine phosphatase activity; and pyrophosphatase activity. Involved in bone mineralization. Acts upstream of or within bone mineralization involved in bone maturation and endochondral ossification. Located in extracellular matrix and extracellular membrane-bounded organelle. Is expressed in several structures, including jaw; limb; liver; skeleton; and spleen. Orthologous to human PHOSPHO1 (phosphoethanolamine/phosphocholine phosphatase 1).
PHENOTYPE: Mice homozygous for an ENU-induced mutation exhibit fractures, bowed long bones, osteomalacia, and scoliosis. [provided by MGI curators]
  • synonyms:
  • DNA segment, Chr 11, KL Mohlke 36,
  • D11Moh36,
  • MGI:1343159,
  • phosphatase, orphan 1,
  • Phospho1
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2 Involved In Mutations

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0 Transgenic Expressors

0 UTRs

Canonical gene --> CDSs in specific strains.

Canonical gene --> Exons in specific strains

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Proteins

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Genes --> Homologs

Interactions

6 Pathways

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Gene --> Protein-Protein Interactions

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Phenotype

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Disease

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