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Allele : Hr<N> lysine demethylase and nuclear receptor corepressor; near naked
Primary Identifier  MGI:1856060 Allele Type  Spontaneous
Gene  Hr Inheritance Mode  Semidominant
Strain of Origin  Not Specified Is Recombinase  false
Is Wild Type  false
molecularNote  This allele comprises a nucleotide transition of A-to-G at position -293 upstream of the start codon in 5' UTR exon 2 results in conversion of a potential upstream open reading frame initiation methionine codon from ATG to GTG.
  • mutations:
  • Single point mutation
  • synonyms:
  • Hr<n>,
  • Hr<n>
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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

5 Publication categories





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