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Protein Coding Gene : Phf7 PHD finger protein 7

Primary Identifier  MGI:1919088 Organism  mouse, laboratory
Chromosome  14 NCBI Gene Number  71838
Mgi Type  protein coding gene
description  FUNCTION: Automated description from the Alliance of Genome Resources (Release 7.1.0)

Predicted to enable metal ion binding activity. Predicted to be located in several cellular components, including Golgi apparatus; cytosol; and nuclear speck. Predicted to be active in nucleus. Orthologous to human PHF7 (PHD finger protein 7).
PHENOTYPE: Mice homozygous for a conditionally allele activated in sperm or a enzymatic dead allele exhibit male infertility associated with oligozoospermia, asthenozoospermia, teratozoospermia, and defective histone to protamine exchange during spermiogenesis. [provided by MGI curators]
  • synonyms:
  • Phf7,
  • 1700010P14Rik,
  • MGI:1916609,
  • AW555949,
  • AI427892,
  • RIKEN cDNA 1700010P14 gene,
  • MGI:2145634,
  • expressed sequence AI427892,
  • RIKEN cDNA 1700006H01 gene,
  • MGI:2145840,
  • 1700006H01Rik,
  • PHD finger protein 7,
  • expressed sequence AW555949

Features --> Cross References

Genome

Sequence Feature Displayer

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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

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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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