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Prickle1m1Ingm
Chemically induced Allele Detail
Summary
Symbol: Prickle1m1Ingm
Name: prickle planar cell polarity protein 1; mutation 1, Ingenium Pharmaceuticals
MGI ID: MGI:4941928
Synonyms: Phe141Ser
Gene: Prickle1  Location: Chr15:93396995-93493772 bp, - strand  Genetic Position: Chr15, 47.69 cM
Alliance: Prickle1m1Ingm page
Mutation
origin
Strain of Origin:  Not Specified
Mutation
description
Allele Type:    Chemically induced (ENU)
Mutation:    Nucleotide substitutions
 
Mutation detailsENU mutagenesis resulted in the amino acid substitution of serine for phenylalanine at position 141 (F141S). (J:169136)
Phenotypes
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View phenotypes and curated references for all genotypes (concatenated display).
Find Mice (IMSR)
Mouse strains and cell lines available from the International Mouse Strain Resource (IMSR)
Carrying this Mutation:  Mouse Strains: 0 strains available      Cell Lines: 0 lines available
Carrying any Prickle1 Mutation:  34 strains or lines available
References
Original:  J:169136 Tao H, et al., Mutations in prickle orthologs cause seizures in flies, mice, and humans. Am J Hum Genet. 2011 Feb 11;88(2):138-49
All:  1 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
12/10/2024
MGI 6.24
The Jackson Laboratory