About   Help   FAQ
Celsr1ctb
Spontaneous Allele Detail
Summary
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
Alliance: Celsr1ctb page
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
Loading...
View phenotypes and curated references for all genotypes (concatenated display).
Expression
In Structures Affected by this Mutation: 4 anatomical structure(s)
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:  143 strains or lines available
References
Original:  J:229303 Harris BS, et al., Two spontaneous alleles of Celsr1. MGI Direct Data Submission. 2016;
All:  3 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)
Citing These Resources
Funding Information
Warranty Disclaimer, Privacy Notice, Licensing, & Copyright
Send questions and comments to User Support.
last database update
04/16/2024
MGI 6.23
The Jackson Laboratory