About   Help   FAQ
Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID
Rnpc3
RNA-binding region (RNP1, RRM) containing 3
MGI:1914475
37 phenotypes from 4 alleles in 4 genetic backgrounds
Export: Excel File
Allelic Composition
Genetic Background
Annotated Term Reference
Ndor1Tg(UBC-cre/ERT2)1Ejb/Ndor1+
Rnpc3tm1c(EUCOMM)Wtsi/Rnpc3+
involves: 129S/SvEv * C57BL/6 * C57BL/6N
no abnormal phenotype detected J:267519
Ndor1Tg(UBC-cre/ERT2)1Ejb/Ndor1+
Rnpc3tm1c(EUCOMM)Wtsi/Rnpc3tm1c(EUCOMM)Wtsi
involves: 129S/SvEv * C57BL/6 * C57BL/6N
abnormal digestive system morphology J:267519
abnormal enterocyte proliferation J:267519
abnormal esophageal squamous epithelium morphology J:267519
abnormal intestinal epithelium morphology J:267519
abnormal intestinal mucosa morphology J:267519
abnormal large intestine crypts of Lieberkuhn morphology J:267519
abnormal skin morphology J:267519
abnormal small intestinal crypt cell proliferation J:267519
abnormal small intestine crypts of Lieberkuhn morphology J:267519
abnormal stomach glandular epithelium morphology J:267519
anemia J:267519
decreased erythrocyte cell number J:267519
decreased leukocyte cell number J:267519
decreased lymphocyte cell number J:267519
decreased monocyte cell number J:267519
decreased small intestinal villus height J:267519
decreased thymus weight J:267519
disheveled coat J:267519
epidermal atrophy J:267519
esophageal inflammation J:267519
hunched posture J:267519
increased small intestinal crypt cell apoptosis J:267519
moribund J:267519
sebaceous gland atrophy J:267519
small intestinal inflammation J:267519
thrombocytopenia J:267519
thymus atrophy J:267519
thymus cortex atrophy J:267519
thymus medulla atrophy J:267519
weight loss J:267519
Rnpc3em1(IMPC)H/Rnpc3em1(IMPC)H
C57BL/6NTac-Rnpc3em1(IMPC)H/H
embryonic lethality prior to organogenesis J:211773
preweaning lethality, complete penetrance J:211773
Rnpc3tm1a(EUCOMM)Wtsi/Rnpc3+
involves: C57BL/6N
no abnormal phenotype detected J:267519
Rnpc3tm1b(EUCOMM)Wtsi/Rnpc3+
involves: C57BL/6N
no abnormal phenotype detected J:267519
Rnpc3tm1b(EUCOMM)Wtsi/Rnpc3tm1b(EUCOMM)Wtsi
involves: C57BL/6N
embryonic lethality before implantation, complete penetrance J:267519
Rnpc3tm1b(EUCOMM)Wtsi/Rnpc3tm1b(EUCOMM)Wtsi
involves: C57BL/6N * FVB
abnormal preimplantation embryo development J:267519
embryonic growth arrest J:267519
failure of blastocyst to hatch from the zona pellucida J:267519

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)
Citing These Resources
Funding Information
Warranty Disclaimer, Privacy Notice, Licensing, & Copyright
Send questions and comments to User Support.
last database update
11/12/2024
MGI 6.24
The Jackson Laboratory