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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID
Rdx
radixin
MGI:97887
20 phenotypes from 2 alleles in 2 genetic backgrounds
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Allelic Composition
Genetic Background
Annotated Term Reference
Rdxtm1.1(KOMP)Vlcg/Rdx+
C57BL/6N-Rdxtm1.1(KOMP)Vlcg/J
increased mean corpuscular hemoglobin J:211773
Rdxtm1.1(KOMP)Vlcg/Rdxtm1.1(KOMP)Vlcg
C57BL/6N-Rdxtm1.1(KOMP)Vlcg/J
female infertility J:211773
preweaning lethality, incomplete penetrance J:211773
Rdxtm1Sts/Rdxtm1Sts
involves: 129S4/SvJae * C57BL/6
abnormal blood homeostasis J:77485
abnormal cochlear hair cell stereociliary bundle morphology J:124151
abnormal inner hair cell stereociliary bundle morphology J:124151
abnormal liver morphology J:77485
abnormal outer hair cell stereociliary bundle morphology J:124151
absent pinna reflex J:124151
cochlear hair cell degeneration J:124151
deafness J:124151
fused inner hair cell stereocilia J:124151
fused outer hair cell stereocilia J:124151
increased circulating alkaline phosphatase level J:77485
increased circulating aspartate transaminase level J:77485
increased circulating bilirubin level J:77485
increased or absent threshold for auditory brainstem response J:124151
organ of Corti degeneration J:124151
short inner hair cell stereocilia J:124151
short outer hair cell stereocilia J:124151

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
04/23/2024
MGI 6.23
The Jackson Laboratory