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Protein Coding Gene : Selenop selenoprotein P
Primary Identifier  MGI:894288 Organism  mouse, laboratory
Chromosome  15 NCBI Gene Number  20363
Mgi Type  protein coding gene
description  FUNCTION: Automated description from the Alliance of Genome Resources (Release 7.1.0)

Enables selenium binding activity. Acts upstream of or within several processes, including brain development; locomotory behavior; and selenium compound metabolic process. Located in extracellular space. Is expressed in several structures, including central nervous system; embryo mesenchyme; extraembryonic component; genitourinary system; and integumental system. Orthologous to human SELENOP (selenoprotein P).
PHENOTYPE: Homozygotes for targeted null mutations exhibit ataxia, spasticity, impaired growth, reduced male fertility, and excess mortality. [provided by MGI curators]
  • synonyms:
  • Selenop,
  • D15Ucla1,
  • expressed sequence AU018766,
  • MGI:90427,
  • selenoprotein P, plasma, 1,
  • selenoprotein P,
  • Se-P,
  • DNA segment, Chr 15, University of California at Los Angeles 1,
  • MGI:2146129,
  • selp,
  • AU018766,
  • Sepp1,
  • MGD-MRK-4226
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Canonical gene --> CDSs in specific strains.

Canonical gene --> Exons in specific strains

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Canonical gene --> Transcripts in specific strains.

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4 Pathways

Trail: ProteinCodingGene

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Gene --> Protein-Protein Interactions

Expression

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Phenotype

Genes/Features --> Phenotypes (MP terms)

Disease

Mouse features --> Human diseases

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