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Otcspf-ash
Spontaneous Allele Detail
Summary
Symbol: Otcspf-ash
Name: ornithine transcarbamylase; abnormal skin and hair
MGI ID: MGI:1856179
Synonyms: spfash, spf-ash
Gene: Otc  Location: ChrX:10118584-10187275 bp, + strand  Genetic Position: ChrX, 4.66 cM, cytoband A1
Alliance: Otcspf-ash page
Mutation
origin
Strain of Origin:  Not Specified
Mutation
description
Allele Type:    Spontaneous (Hypomorph)
Mutation:    Single point mutation
 
Mutation detailsA G-to-A missense transition of the last nucleotide of exon 4 changes an arginine to histidine (p.R129H) and results in inefficient mRNA splicing at this site, as well as at a site located 48 bases into the adjacent intron. This allele is hypomorphic; approximately 5-10% of wild-type hepatic enzyme activity is retained. (J:9817)
Inheritance:    Semidominant
Phenotypes
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View phenotypes and curated references for all genotypes (concatenated display).
Disease models
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Expression
In Mice Carrying this Mutation: 31 assay results
In Structures Affected by this Mutation: 5 anatomical structure(s)
Find Mice (IMSR)
Mouse strains and cell lines available from the International Mouse Strain Resource (IMSR)
Carrying this Mutation:  Mouse Strains: 1 strain available      Cell Lines: 0 lines available
Carrying any Otc Mutation:  22 strains or lines available
References
Original:  J:5476 Doolittle DP, et al., A new allele of the sparse fur gene in the mouse. J Hered. 1974 May-Jun;65(3):194-5
All:  31 reference(s)

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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last database update
04/16/2024
MGI 6.23
The Jackson Laboratory