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Protein Coding Gene : Ift52 intraflagellar transport 52
Primary Identifier  MGI:2387217 Organism  mouse, laboratory
Chromosome  2 NCBI Gene Number  245866
Mgi Type  protein coding gene
description  FUNCTION: Automated description from the Alliance of Genome Resources (Release 8.0.0)

Acts upstream of or within several processes, including embryonic morphogenesis; negative regulation of keratinocyte proliferation; and non-motile cilium assembly. Located in several cellular components, including ciliary base; ciliary tip; and microtubule organizing center. Part of intraciliary transport particle B. Human ortholog(s) of this gene implicated in asphyxiating thoracic dystrophy. Orthologous to human IFT52 (intraflagellar transport 52).
PHENOTYPE: Mice homozygous for a transgenic gene disruption exhibit embryonic lethality between E9 and E10. [provided by MGI curators]
  • synonyms:
  • Ift52,
  • cDNA sequence BC037708,
  • NGD5,
  • BC037708,
  • intraflagellar transport 52,
  • MGC:47065
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Canonical gene --> Exons in specific strains

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Canonical gene --> Transcripts in specific strains.

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6 Pathways

Trail: ProteinCodingGene

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