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Pfn4em2Hsc
Endonuclease-mediated Allele Detail
Summary
Symbol: Pfn4em2Hsc
Name: profilin family, member 4; endonuclease-mediated mutation 2, Hubert Schorle
MGI ID: MGI:6718279
Synonyms: Pfn4deltab
Gene: Pfn4  Location: Chr12:4819022-4828813 bp, + strand  Genetic Position: Chr12, 2.09 cM, cytoband A1.1
Alliance: Pfn4em2Hsc page
Mutation
origin
Strain of Origin:  C57BL/6J
Mutation
description
Allele Type:    Endonuclease-mediated (Null/knockout)
Mutation:    Intragenic deletion
 
Mutation detailsCRISPR-targeting of exons 2 through 4 deleted 5417 bp leading to generation of a 5' truncated nonsense protein. qRT-PCR analysis confirmed the absence of mRNA expression in the testes of homozygous mutant males. (J:328252)
Phenotypes
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View phenotypes and curated references for all genotypes (concatenated display).
Expression
In Structures Affected by this Mutation: 2 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 Pfn4 Mutation:  18 strains or lines available
References
Original:  J:328252 Umer N, et al., PFN4 is required for manchette development and acrosome biogenesis during mouse spermiogenesis. Development. 2022 Aug 15;149(16):dev200499
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