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Allele : Hr<rh-R> lysine demethylase and nuclear receptor corepressor; rhino Oak Ridge

Primary Identifier  MGI:3580645 Allele Type  Spontaneous
Gene  Hr Inheritance Mode  Recessive
Strain of Origin  Mixed stock Is Recombinase  false
Is Wild Type  false
description  Direct Submssion mutation arose on a (JH x Sb)F1 where JH is a (C3H/Rl x 101)F1 and Sb is a (SEC/El x C57BL/RlEl)F1 and then maintained on a C3H/Rl x C57BL/10Rl background. (J:156918)
molecularNote  A single nucleotide change (from C to T) was identified at coding nucleotide 2440. This change in exon 12 causes a premature stop codon at arginine 814 (p.R814*).
  • mutations:
  • Single point mutation
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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

3 Publication categories