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Allele : Smarca4<tm1.2Pcn> SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 4; targeted mutation 1.2, Pierre Chambon

Primary Identifier  MGI:3605892 Allele Type  Targeted
Attribute String  Conditional ready, No functional change Gene  Smarca4
Transmission  Germline Strain of Origin  129S2/SvPas
Is Recombinase  false Is Wild Type  false
description  Phenotypic Similarity to Human Syndrome: Aortic Valve Disease J:226941 in mice homozygous for Smarca4tm1.2Pcn and heterozygous for either Nfatc1tm1(cre)Bz or Nfatc1tm1.1(cre)Bz.
molecularNote  A single loxP site was inserted upstream of exon 18 and a floxed hygromycin resistance cassette was inserted downstream of exon 19. The hygromycin resistance cassette was selectively excised from correctly targeted ES cells by transient transfection with a cre-expression vector. Exons 18 and 19, encoding part of the ATPase-helicase motifs, were thus flanked by loxP sites in the resulting ES cells.
  • mutations:
  • Insertion
  • synonyms:
  • Smarca4<tm1Grc>,
  • SNF2Beta<L:La>,
  • brg1<FL>,
  • Brg1<lox>,
  • Brg1<L2>,
  • SNF2Beta<L:La>,
  • Smarca4<tm1Grc>,
  • brg1<FL>,
  • Smarca4<tm1Pcn>,
  • Brg1<F>,
  • Brg1<F>,
  • Brg1<L2>,
  • Smarca4<tm1Pcn>,
  • Brg1<lox>
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1 Feature

Genome

0 Expresses

0 Mutation Involves

Phenotype

Mouse alleles --> Mammalian phenotypes (MP terms)

 

Other

1 Carried By

0 Driven By

111 Publication categories