Hr^N
Spontaneous Allele Detail

Summary

• Symbol: Hr^N
• Name: lysine demethylase and nuclear receptor corepressor; near naked
• MGI ID: MGI:1856060
• Synonyms: Hrⁿ
• Gene: Hr Location: Chr14:70789652-70810988 bp, + strand Genetic Position: Chr14, 36.32 cM
• Alliance: Hr^N page

Mutation origin

• Strain of Origin: Not Specified

Mutation description

• Allele Type: Spontaneous
• Mutation: Single point mutation
• Mutation details: 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. (J:122083, J:150720)
• Inheritance: Semidominant

Expression

In Mice Carrying this Mutation:	1 RNA-Seq or microarray experiment(s)
In Structures Affected by this Mutation:	2 anatomical structure(s)

Find Mice (IMSR)

• Mouse strains and cell lines available from the International Mouse Strain Resource (IMSR)
• Carrying this Mutation: Mouse Strains: 2 strains available Cell Lines: 0 lines available
• Carrying any Hr Mutation: 87 strains or lines available

References

• Original: J:7103 Stelzner KF, Four dominant autosomal mutations affecting skin and hair development in the mouse. J Hered. 1983 May-Jun;74(3):193-6
• All: 4 reference(s)