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Allele : t<w5> t-complex; t, wild 5

Primary Identifier  MGI:1856570 Allele Type  Spontaneous
Gene  t Inheritance Mode  Recessive
Strain of Origin  wild-derived Is Recombinase  false
Is Wild Type  false
description  This homozygous lethal allele originated in a mouse caught in the New York suburbs. It suppresses recombination and is a member of the complementation group: tw5 ,tw6 ,tw10 ,tw11 ,tw13 ,tw14 ,tw15 ,tw16 ,tw17 ,tw37 , tw38 ,tw39 ,tw41 ,tw46 ,tw47 ,tw74 ,tw75 ,tw80 ,tw81. T/tw5 phenotype is tail-less.
    Embryos homozygous for tw5 arrest at gastrulation and exhibit defects in proliferation/differentiation of embryonic ectoderm.
molecularNote  This t haplotype includes a mutation in Vps52, Vps52t-w5 that inserts 2 G nucleotides at the start of exon 2 in a stretch of consecutive G nucleotides (9 in the wild-type C57BL/6 sequence) resulting in a frameshift mutation that generates a premature termination codon. The mutation in Vsp52 is responsible for the embryonic lethal homozygous phenotype in this haplotype.
  • mutations:
  • Nucleotide repeat expansion,
  • Inversion
  • synonyms:
  • t-complex lethal w5,
  • tcl-w5,
  • t-complex lethal w5,
  • tcl-w5
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1 Feature

Genome

0 Expresses

0 Mutation Involves

Phenotype

Mouse alleles --> Mammalian phenotypes (MP terms)

 

Other

24 Carried By

0 Driven By

21 Publication categories