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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID
Rnaseh2b
ribonuclease H2, subunit B
MGI:1914403
17 phenotypes from multigenic genotypes
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Allelic Composition
Genetic Background
Annotated Term Reference
Ifnar1tm1Agt/Ifnar1tm1Agt
Rnaseh2btm1a(EUCOMM)Wtsi/Rnaseh2btm1a(EUCOMM)Wtsi
involves: 129S2/SvPas * C57BL/6N
decreased fetal size J:186986
perinatal lethality, complete penetrance J:186986
Rnaseh2bem1Anu/Rnaseh2b+
Tlr7em2Anu/Tlr7+
C57BL/6NCrl-Rnaseh2bem1Anu Tlr7em2Anu
abnormal immune system morphology J:324448
abnormal mature B cell morphology J:324448
increased autoantibody level J:324448
increased CD4-positive, alpha-beta T cell number J:324448
increased germinal center B cell number J:324448
increased plasma cell number J:324448
increased T follicular helper cell number J:324448
Rnaseh2btm1a(EUCOMM)Wtsi/Rnaseh2btm1a(EUCOMM)Wtsi
Trp53tm1Mlh/Trp53tm1Mlh
involves: 129P2/OlaHsd * C57BL/6N
abnormal cell nucleus morphology J:186180
abnormal neural tube closure J:186180
normal cellular phenotype J:186180
chromosomal instability J:186180
decreased embryo size J:186180
normal embryo phenotype J:186180
embryonic growth retardation J:186180
increased cellular sensitivity to alkylating agents J:186180

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
04/30/2024
MGI 6.23
The Jackson Laboratory