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Allele : Alx4<lst> aristaless-like homeobox 4; Strong's luxoid

Primary Identifier  MGI:1856068 Allele Type  Chemically induced (other)
Gene  Alx4 Inheritance Mode  Semidominant
Strain of Origin  NHO/Brpb Is Recombinase  false
Is Wild Type  false
description  This mutation arose after treatment of mice with methylcholanthrene.
molecularNote  The G to A transition point mutation in codon 206 is predicted to alter amino acid arginine to glutamine in the corresponding amino acid located in the homeodomain.
  • mutations:
  • Single point mutation
  • synonyms:
  • Springville luxoid,
  • lst<D>,
  • Springville luxoid,
  • lst<D>
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1 Feature

Genome

0 Expresses

0 Mutation Involves

Phenotype

Mouse alleles --> Mammalian phenotypes (MP terms)

 

Other

0 Carried By

0 Driven By

17 Publication categories