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Prm2em2Hsc
Endonuclease-mediated Allele Detail
Summary
Symbol: Prm2em2Hsc
Name: protamine 2; endonuclease-mediated mutation 2, Hubert Schorle
MGI ID: MGI:5770554
Synonyms: Prm2delta101
Gene: Prm2  Location: Chr16:10609241-10609969 bp, - strand  Genetic Position: Chr16, 5.84 cM
Alliance: Prm2em2Hsc page
Mutation
origin
Strain of Origin:  (C57BL/6 x DBA)F2
Mutation
description
Allele Type:    Endonuclease-mediated (Null/knockout)
Mutation:    Intragenic deletion
 
Mutation detailsCRISPR/Cas9-mediated genome editing generated a 101bp deletion in exon 1 leading to a frameshift that results in nonsense transcripts with a premature stop codon after amino acid 23. Western blot analysis of basic nuclear proteins isolated from epididymal sperm confirmed the absence of detectable mature protein in homozygous mutant males. (J:243626)
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 Prm2 Mutation:  8 strains or lines available
References
Original:  J:243626 Schneider S, et al., Re-visiting the Protamine-2 locus: deletion, but not haploinsufficiency, renders male mice infertile. Sci Rep. 2016 Nov 11;6:36764
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
04/23/2024
MGI 6.23
The Jackson Laboratory