Faculty Research 1990 - 1999
The mouse mutation ulnaless on chromosome 2.
Document Type
Article
Publication Date
1990
Keywords
Chromosome-Mapping, Crosses-Genetic, Extremities, Female, Heterozygote, Linkage-(Genetics), Male, Mice, Mice-Inbred-Strains, Mutation, Phenotype, Reproduction, Support-Non-U, S, -Gov't, Support-U, S, -Gov't-Non-P, H, S, Support-U, S, -Gov't-P, H, S
First Page
151
Last Page
153
JAX Location
1,952.
JAX Source
J Hered 1990 Mar-Apr;81(2):151-3.
Grant
RR01183, CA34196
Abstract
The dominant skeletal mutation ulnaless (Ul) in the mouse causes extreme reduction of the radius and ulna and deformities of the tibia and fibula. Penetrance appears to be complete, but the homozygote is not known, as heterozygous males do not breed. We report the linkage of the Ul gene on Chromosome 2, 18 cM proximal to pallid (pa), and describe its phenotypic effects.
Recommended Citation
Davisson MT,
Cattanach BM.
The mouse mutation ulnaless on chromosome 2. J Hered 1990 Mar-Apr;81(2):151-3.