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Ripk1em2Xlin
Endonuclease-mediated Allele Detail
Summary
Symbol: Ripk1em2Xlin
Name: receptor (TNFRSF)-interacting serine-threonine kinase 1; endonuclease-mediated mutation 2, Xin Lin
MGI ID: MGI:6363438
Synonyms: Ripk1-
Gene: Ripk1  Location: Chr13:34186346-34221130 bp, + strand  Genetic Position: Chr13, 14.01 cM
Alliance: Ripk1em2Xlin page
Mutation
origin
Strain of Origin:  C57BL/6
Mutation
description
Allele Type:    Endonuclease-mediated (Null/knockout)
Mutation:    Nucleotide substitutions
 
Mutation detailsUsing CRISPR/Cas9 technology with an sgRNA targeting the sequence around aspartic acid codon 367, an allele was created with a p.D367* premature stop codon mutation in the Intermediate Domain. (J:279494)
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 Ripk1 Mutation:  32 strains or lines available
References
Original:  J:279494 Tang Y, et al., K63-linked ubiquitination regulates RIPK1 kinase activity to prevent cell death during embryogenesis and inflammation. Nat Commun. 2019 Sep 13;10(1):4157
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
01/06/2026
MGI 6.24
The Jackson Laboratory