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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID
Xrcc1
X-ray repair complementing defective repair in Chinese hamster cells 1
MGI:99137
41 phenotypes from 2 alleles in 6 genetic backgrounds
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Allelic Composition
Genetic Background
Annotated Term Reference
Alpltm1(cre)Nagy/Alpl+
Xrcc1tm1Pmc/Xrcc1tm1Pmc
involves: 129S1/Sv * 129X1/SvJ
abnormal mitochondrial ATP synthesis coupled electron transport J:292217
abnormal mitochondrial morphology J:292217
abnormal mitochondrial physiology J:292217
abnormal seminiferous tubule epithelium morphology J:292217
abnormal seminiferous tubule morphology J:292217
abnormal spermatocyte morphology J:292217
abnormal spermatogenesis J:292217
abnormal spermatogonia morphology J:292217
asthenozoospermia J:292217
decreased catalase activity J:292217
decreased testis weight J:292217
increased testis apoptosis J:292217
male infertility J:292217
oligozoospermia J:292217
oxidative stress J:292217
small testis J:292217
Meox2tm1(cre)Sor/Meox2+
Xrcc1tm1Pmc/Xrcc1tm1Pmc
involves: 129S1/Sv * 129S4/SvJaeSor * C57BL/6
abnormal embryonic tissue morphology J:152528
embryonic lethality during organogenesis, complete penetrance J:152528
increased embryonic tissue cell apoptosis J:152528
Xrcc1tm1Pmc/Xrcc1tm1Pmc
involves: 129S1/Sv * C57BL/6
no abnormal phenotype detected J:152528
Xrcc1tm1Pmc/Xrcc1tm1Pmc
Tg(Nes-cre)1Kln/0
involves: 129S1/Sv * C57BL/6 * SJL
abnormal brain interneuron morphology J:152528
abnormal brain white matter morphology J:152528
abnormal DNA repair J:145730, J:152528
abnormal neuron differentiation J:152528
ataxia J:152528
normal cellular phenotype J:226703
decreased body size J:152528
decreased body weight J:152528
decreased brain size J:152528
increased neuron apoptosis J:152528
loss of GABAergic neurons J:152528
postnatal growth retardation J:152528
premature death J:152528
seizures J:152528
small cerebellum J:152528
Xrcc1tm1Pmc/Xrcc1tm1Pmc
Tg(Nes-cre)1Kln/0
involves: 129S1/Sv * FVB/N
abnormal DNA repair J:170077
Xrcc1tm1Rpe/Xrcc1tm1Rpe
involves: 129X1/SvJ
abnormal endoderm development J:54226
absent mesoderm J:54226
decreased embryo size J:54226
normal embryo phenotype J:54226
embryonic lethality between somite formation and embryo turning, complete penetrance J:54226
failure to gastrulate J:54226

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
04/09/2024
MGI 6.23
The Jackson Laboratory