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Allele : Vsx2<or-J> visual system homeobox 2; ocular retardation Jackson
Primary Identifier  MGI:1856112 Allele Type  Spontaneous
Gene  Vsx2 Inheritance Mode  Recessive
Strain of Origin  129S1/Sv-Oca2<+> Tyr<+> Kitl<Sl> Is Recombinase  false
Is Wild Type  false
molecularNote  The molecular mutation is a premature stop codon in exon 3, corresponding to the homeobox domain of the encoded protein.
  • mutations:
  • Nucleotide substitutions
  • synonyms:
  • orJ,
  • Chx10<->,
  • orJ,
  • Chx10<->
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1 Feature

Genome

0 Expresses

0 Mutation Involves

Phenotype

Mouse alleles --> Mammalian phenotypes (MP terms)

 

Other

9 Carried By

0 Driven By

40 Publication categories





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