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Allele : Msx2<tm1Rilm> msh homeobox 2; targeted mutation 1, Richard Maas
Primary Identifier  MGI:1926381 Allele Type  Targeted
Attribute String  Null/knockout Gene  Msx2
Inheritance Mode  Recessive Transmission  Germline
Strain of Origin  129S4/SvJae Is Recombinase  false
Is Wild Type  false
description  Phenotypic Similarity to Human Syndrome: Peters anomaly in homozygous mice (J:184697)
molecularNote  Gene disruption caused by insertion of a pMC1-neo cassette into coding sequences located just 5' to the homeobox domain in exon 2.
  • mutations:
  • Insertion
  • synonyms:
  • Msx2-,
  • Msx2-
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1 Feature

Trail: Allele

Genome

0 Expresses

0 Mutation Involves

Phenotype

Mouse alleles --> Mammalian phenotypes (MP terms)

 

Other

2 Carried By

Trail: Allele

0 Driven By

35 Publication categories

Trail: Allele




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