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Protein Coding Gene : Spatc1l spermatogenesis and centriole associated 1 like

Primary Identifier  MGI:1923823 Organism  mouse, laboratory
Chromosome  10 NCBI Gene Number  76573
Mgi Type  protein coding gene
description  FUNCTION: Automated description from the Alliance of Genome Resources (Release 8.0.0)

Enables protein kinase A regulatory subunit binding activity. Acts upstream of or within several processes, including actin polymerization or depolymerization; positive regulation of cAMP-dependent protein kinase activity; and positive regulation of cAMP/PKA signal transduction. Located in centrosome and sperm head-tail coupling apparatus. Is expressed in several structures, including alimentary system; genitourinary system; heart; nervous system; and sensory organ. Orthologous to human SPATC1L (spermatogenesis and centriole associated 1 like).
PHENOTYPE: Male mice homozygous for a null mutation are infertile with acephalic sperm and detached sperm tails. Male mice heterozygous for a null mutation display reduced fertility with similar sperm abnormalities. [provided by MGI curators]
  • synonyms:
  • Spatc1l,
  • spermatogenesis and centriole associated 1 like,
  • MGI:2652136,
  • EST AA062323,
  • AA062323,
  • RIKEN cDNA 1700022B01 gene,
  • 1700027D21Rik,
  • MGI:1916661,
  • RIKEN cDNA 1700027D21 gene,
  • 1700022B01Rik

Features --> Cross References

Genome

Sequence Feature Displayer

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0 Canonical

0 CDSs

0 Exons

0 Genomic Clusters

5 Involved In Mutations

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

0 Pathways

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Gene --> Protein-Protein Interactions

Expression

Gene --> Expression annotations

Phenotype

Genes/Features --> Phenotypes (MP terms)

Disease

Mouse features --> Human diseases

Literature

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0 Driver For