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Frey1tm2Osb
Endonuclease-mediated Allele Detail
Summary
Symbol: Frey1tm2Osb
Name: Frey regulator of sperm-oocyte fusion 1; endonuclease-mediated mutation 2, Research Institute for Microbial Diseases, Osaka University
MGI ID: MGI:7495886
Synonyms: 1700029I15Rikdelta
Gene: Frey1  Location: Chr2:92213263-92213948 bp, + strand  Genetic Position: Chr2, 50.99 cM
Alliance: Frey1tm2Osb page
Mutation
origin
Strain of Origin:  C57BL/6J
Mutation
description
Allele Type:    Endonuclease-mediated (Null/knockout)
Mutation:    Intragenic deletion
 
Mutation detailsCRISPR/Cas9 genome editing technology was used to generate a 215 bp deletion at the first coding exon. (J:337566)
Phenotypes
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View phenotypes and curated references for all genotypes (concatenated display).
Expression
In Structures Affected by this Mutation: 1 anatomical structure(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 Frey1 Mutation:  8 strains or lines available
References
Original:  J:337566 Lu Y, et al., 1700029I15Rik orchestrates the biosynthesis of acrosomal membrane proteins required for sperm-egg interaction. Proc Natl Acad Sci U S A. 2023 Feb 21;120(8):e2207263120
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
04/23/2024
MGI 6.23
The Jackson Laboratory