Summary | Mutation origin | Mutation description | Expression | Phenotypes | Find Mice (IMSR) | References

Symbol:	HrN
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:	HrN page

Strain of Origin:

Not Specified

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

View phenotypes and curated references for all genotypes (concatenated display).

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

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:	84 strains or lines available

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)