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Pcdha9em1Clo
Endonuclease-mediated Allele Detail
Summary
Symbol: Pcdha9em1Clo
Name: protocadherin alpha 9; endonuclease-mediated mutation 1, Cecilia Lo
MGI ID: MGI:5805231
Gene: Pcdha9  Location: Chr18:37130933-37320710 bp, + strand  Genetic Position: Chr18, 19.46 cM
Alliance: Pcdha9em1Clo page
Mutation
origin
Strain of Origin:  C57BL/6J
Mutation
description
Allele Type:    Endonuclease-mediated (Not Specified)
Mutations:    Intragenic deletion, Nucleotide substitutions
 
Mutation detailsCRISPR/Cas9 and a donor sequence were used to generate this allele, which has the aspartic acid at residue 796 replaced with valine and the leucine and methionine at amino acids 797 and 798 deleted. (J:242757)
Inheritance:    Not Specified
Phenotypes
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View phenotypes and curated references for all genotypes (concatenated display).
Disease models
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Expression
In Mice Carrying this Mutation: 1 RNA-Seq or microarray experiment(s)
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 Pcdha9 Mutation:  45 strains or lines available
References
Original:  J:242757 Liu X, et al., The complex genetics of hypoplastic left heart syndrome. Nat Genet. 2017 Jul;49(7):1152-1159
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
04/16/2024
MGI 6.23
The Jackson Laboratory