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Celsr1ctb
Spontaneous Allele Detail
Nomenclature
Symbol: Celsr1ctb
Name: cadherin, EGF LAG seven-pass G-type receptor 1; curly tail bobber
MGI ID: MGI:5577174
Gene: Celsr1  Location: Chr15:85783130-85918404 bp, - strand  Genetic Position: Chr15, 40.42 cM
Mutation
origin
Strain of Origin:  CByJ.Cg-Foxn1nu/J
Mutation
description
Allele Type:    Spontaneous (Null/knockout)
Mutation:    Intragenic deletion
 
Mutation detailsThis spontaneous single-nucleotide deletion of G (C forward strand) at chromosome 15 position 85,959,170 bp (GRCm38) causes a frameshift and subsequent premature stop codon. (J:222308, J:229303)
Inheritance:    Recessive
Phenotypes
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View phenotypes and curated references for all genotypes (concatenated display).
Expression
In Structures Affected by this Mutation: 6 anatomical structures
Find Mice (IMSR)
Mouse strains and cell lines available from the International Mouse Strain Resource (IMSR)
Carrying this Mutation:  Mouse Strains: 1 strain available      Cell Lines: 0 lines available
Carrying any Celsr1 Mutation:  68 strains or lines available
References
Original:  J:229303 Harris BS, et al., Two spontaneous alleles of Celsr1. MGI Direct Data Submission. 2016;
All:  2 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
11/30/2021
MGI 6.17
The Jackson Laboratory