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Phenotypes Associated with This Genotype
Genotype
MGI:3588036
Allelic
Composition
Pou3f4Slf/Y
Genetic
Background
C3H101H-Pou3f4Slf
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Pou3f4Slf mutation (2 available); any Pou3f4 mutation (4 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
behavior/neurological
• slight up and down shaking, most easily identifiable around weaning age

hearing/vestibular/ear
• fibrocyte abnormalities in the spiral ligament

skeleton
• fibrocyte abnormalities in the spiral ligament

Mouse Models of Human Disease
OMIM ID Ref(s)
Deafness, X-Linked 2; DFNX2 304400 J:59387


Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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last database update
06/22/2016
MGI 6.04
The Jackson Laboratory