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Phenotypes Associated with This Genotype
Genotype
MGI:5648857
Allelic
Composition
Prickle1tm1Asw/Prickle1tm1.2Asw
Genetic
Background
Not Specified
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Prickle1tm1.2Asw mutation (0 available); any Prickle1 mutation (28 available)
Prickle1tm1Asw mutation (0 available); any Prickle1 mutation (28 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
craniofacial
• fused mandibular incisors
• flat nose

growth/size/body
• fused mandibular incisors
• flat nose

limbs/digits/tail
• shortened digital bones

skeleton
• fused mandibular incisors
• shortened long bones and digital bones
• incomplete and distorted vertebrae formation in the spinal cord

vision/eye
• abnormal appearance of eyelid and eyelashes

Mouse Models of Human Disease
DO ID OMIM ID(s) Ref(s)
autosomal recessive Robinow syndrome DOID:0060764 OMIM:268310
J:213772


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
11/22/2022
MGI 6.22
The Jackson Laboratory