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Protein Coding Gene : Styx serine/threonine/tyrosine interaction protein
Primary Identifier  MGI:1891150 Organism  mouse, laboratory
Chromosome  14 NCBI Gene Number  56291
Mgi Type  protein coding gene
description  FUNCTION: Automated description from the Alliance of Genome Resources (Release 8.0.0)

Predicted to enable F-box domain binding activity and pseudophosphatase activity. Acts upstream of or within spermatogenesis. Located in cytoplasm. Orthologous to human STYX (serine/threonine/tyrosine interacting protein).
PHENOTYPE: Males homozygous for a targeted null mutation are sterile due to a deficiency of germ cells at the immature, round, and elongating spermatid stages. Residual epididymal sperm have head abnormalities. [provided by MGI curators]
  • synonyms:
  • RIKEN cDNA 0610039A20 gene,
  • serine/threonine/tyrosine interaction protein,
  • 0610039A20Rik,
  • STNS (alternatively spliced intron of Styx),
  • MGI:1918939,
  • Styx
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1 Involved In Mutations

Trail: ProteinCodingGene

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Canonical gene --> CDSs in specific strains.

Canonical gene --> Exons in specific strains

Canonical gene --> Strain-specific IDs, biotypes, and locations

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Features --> Overlapping features

Proteins

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Gene --> Protein-Protein Interactions

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Disease

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