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Phenotypes Associated with This Genotype
Genotype
MGI:3851518
Allelic
Composition
Whsc1tm1Ykan/Whsc1+
Genetic
Background
involves: 129S2/SvPas * C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Whsc1tm1Ykan mutation (0 available); any Whsc1 mutation (17 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
growth/size/body
• some mice exhibit severe growth retardation

cardiovascular system
• hypoplasia of the septum secundum was observed more frequently in E18.5 embryos than in controls

craniofacial
• some mice have malocclusions

skeleton
• some mice have malocclusions
• mice have a delay in development of sternum ossifications

Mouse Models of Human Disease
OMIM ID Ref(s)
Wolf-Hirschhorn Syndrome; WHS 194190 J:150360


Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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Funding Information
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last database update
09/20/2016
MGI 6.05
The Jackson Laboratory