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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID
Msn
moesin
MGI:97167
19 phenotypes from 2 alleles in 2 genetic backgrounds
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Allelic Composition
Genetic Background
Annotated Term Reference
Msntm1b(EUCOMM)Hmgu/Y
C57BL/6N-Msntm1b(EUCOMM)Hmgu/J
decreased erythrocyte cell number J:211773
decreased hematocrit J:211773
decreased hemoglobin content J:211773
impaired pupillary reflex J:211773
increased mean corpuscular hemoglobin J:211773
Msntm1b(EUCOMM)Hmgu/Msntm1b(EUCOMM)Hmgu
C57BL/6N-Msntm1b(EUCOMM)Hmgu/J
decreased erythrocyte cell number J:211773
decreased hematocrit J:211773
decreased hemoglobin content J:211773
decreased leukocyte cell number J:211773
increased heart weight J:211773
increased mean corpuscular hemoglobin J:211773
increased mean corpuscular volume J:211773
thrombocytopenia J:211773
Msntm1Sts/Y
involves: 129S4/SvJae * C57BL/6
decreased B cell number J:189837
decreased CD4-positive, alpha-beta T cell number J:189837
decreased eosinophil cell number J:189837
decreased lymphocyte cell number J:189837
decreased neutrophil cell number J:189837
dilated respiratory conducting tube J:141982
impaired leukocyte migration J:189837
increased susceptibility to injury J:141982
no abnormal phenotype detected J:52936
overexpanded pulmonary alveolus J:141982
Msntm1Sts/Msntm1Sts
involves: 129S4/SvJae * C57BL/6
no abnormal phenotype detected J:52936

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
12/10/2024
MGI 6.24
The Jackson Laboratory