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Rnaseh2atm2.1Crh
Targeted Allele Detail
Summary
Symbol: Rnaseh2atm2.1Crh
Name: ribonuclease H2, large subunit; targeted mutation 2.1, Robert J Crouch
MGI ID: MGI:7311689
Synonyms: Rnaseh2aP40D-Y211A, Rnaseh2aRED
Gene: Rnaseh2a  Location: Chr8:85683239-85694498 bp, - strand  Genetic Position: Chr8, 41.38 cM, cytoband C3
Alliance: Rnaseh2atm2.1Crh page
Mutation
origin
Germline Transmission:  Earliest citation of germline transmission: J:270825
Parent Cell Line:  Not Specified (ES Cell)
Strain of Origin:  C57BL/6N
Mutation
description
Allele Type:    Targeted (Not Specified)
Mutations:    Insertion, Nucleotide substitutions
 
Mutation detailsThe targeting construct introduced mutations that resulted in the amino acid substitutions of proline with aspartic acid at position 40 (P40D) and tyrosine with alanine at position 211 (Y211A). Flp-mediated recombination removed the FRT-flanked hygromycin resistance cassette. (J:270825)
Expression
In Mice Carrying this Mutation: 24 assay results
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 Rnaseh2a Mutation:  45 strains or lines available
References
Original:  J:270825 Uehara R, et al., Two RNase H2 Mutants with Differential rNMP Processing Activity Reveal a Threshold of Ribonucleotide Tolerance for Embryonic Development. Cell Rep. 2018 Oct 30;25(5):1135-1145.e5
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
05/07/2024
MGI 6.23
The Jackson Laboratory