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Sprnem1Jvt
Endonuclease-mediated Allele Detail
Summary
Symbol: Sprnem1Jvt
Name: shadow of prion protein; endonuclease-mediated mutation 1, JL Vilotte
MGI ID: MGI:6694148
Synonyms: Sprn0
Gene: Sprn  Location: Chr7:139730541-139734572 bp, - strand  Genetic Position: Chr7, 85.17 cM
Alliance: Sprnem1Jvt page
Mutation
origin
Strain of Origin:  FVB/NJ
Mutation
description
Allele Type:    Endonuclease-mediated (Null/knockout)
Mutation:    Intragenic deletion
 
Mutation detailsZFN-targeting of the open reading frame produced a 1 nt deletion that results in a frameshift and early premature stop codon. (J:289583)
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 Sprn Mutation:  12 strains or lines available
References
Original:  J:289583 Passet B, et al., The Prion-like protein Shadoo is involved in mouse embryonic and mammary development and differentiation. Sci Rep. 2020 Apr 21;10(1):6765
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
12/10/2024
MGI 6.24
The Jackson Laboratory