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Allele : Dspd dominant spermiogenesis defect; dominant spermiognenesis defect

Primary Identifier  MGI:3052992 Allele Type  Transgenic
Gene  Dspd Strain of Origin  (C57BL/6 x C3H)F1
Is Recombinase  false Is Wild Type  false
molecularNote  A transgene insertion resulted in a translocation between chromosomes 7F and 14C and a deletion on chromosome 7C of at least 1 Mb. This deletion contains at least 6 genes including; Cttn, Fadd, Fgf3, Fgf4, Fgf15, and Ccnd1. The transgene contained a chicken Actb promoter, CMV-IE enhancer and a full length human PEG8 cDNA. Expression of the transgene is not thought to be involved in this phenotype.
  • mutations:
  • Intergenic deletion,
  • Translocation
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1 Feature

Trail: Allele

Genome

0 Expresses

0 Mutation Involves

Phenotype

Mouse alleles --> Mammalian phenotypes (MP terms)

 

Other

1 Carried By

Trail: Allele

0 Driven By

3 Publication categories

Trail: Allele