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Allele : Hr<Tg5053Mm> lysine demethylase and nuclear receptor corepressor; transgene insertion 5053, Miriam Meisler

Primary Identifier  MGI:1858045 Allele Type  Transgenic
Gene  Hr Inheritance Mode  Recessive
Strain of Origin  (C57BL/6 x C3H/He)F2 Is Recombinase  false
Is Wild Type  false
description  PCR analysis of flanking markers suggest that the transgene insertion site occurred in the C57BL/6J parent. This allele of Hr was induced by transgenic insertion of a construct with an amylase/elastase enhancer/promotor directing expression of the bacterial chloramphenicolacetyl transferase reporter gene. The clinical and histological phenotype of this mutant closely resembles the phenotype of rhino allele mutants (J:15642).
molecularNote  This allele was initially defined by a noncomplementation test with hr and subsequently found to be the result of the integration of a 2 kb construct, M2CAT ,containing an amylase/elastase enhancer/promoter, between intron 5 and exon 8 of the hairless gene, and deletion of the 3-prime portion of the gene
  • mutations:
  • Insertion
  • synonyms:
  • hr<TgN5053Mm>,
  • hr<TgN5053Mm>
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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

5 Publication categories

Trail: Allele