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Protein Coding Gene : Cep41 centrosomal protein 41
Primary Identifier  MGI:1891414 Organism  mouse, laboratory
Chromosome  6 NCBI Gene Number  83922
Mgi Type  protein coding gene
description  FUNCTION: Automated description from the Alliance of Genome Resources (Release 7.1.0)

Involved in cilium assembly. Located in centriole and ciliary basal body. Is expressed in integumental system muscle. Human ortholog(s) of this gene implicated in Joubert syndrome 15. Orthologous to human CEP41 (centrosomal protein 41).
PHENOTYPE: Homozygous disruption of this gene causes an abnormal gait, increased thermal nociceptive threshold, and alterations in fertility/fecundity and eye morphology. Some embryos homozygous for a gene trapped allele die at E10-E12 exhibiting turning failure, dilated pericardial sacs, and brain anomalies. [provided by MGI curators]
  • synonyms:
  • 2810431D15Rik,
  • MGI:1925624,
  • testis specific gene A14,
  • Tsga14,
  • RIKEN cDNA 2810431D15 gene,
  • MGI:1916627,
  • EST AI449046,
  • centrosomal protein 41,
  • AI503610,
  • RIKEN cDNA 1700017E11 gene,
  • Cep41,
  • AI449046,
  • expressed sequence AI503610,
  • MGI:1889830,
  • 1700017E11Rik,
  • MGI:2141435
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