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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID
Lsm1
LSM1 homolog, mRNA degradation associated
MGI:1914457
15 phenotypes from 1 allele in 1 genetic background
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Allelic Composition
Genetic Background
Annotated Term Reference
Lsm1tm1b(EUCOMM)Hmgu/Lsm1+
C57BL/6N-Lsm1tm1b(EUCOMM)Hmgu/Ieg
abnormal lens morphology J:211773
dilated aorta J:211773
increased circulating sodium level J:211773
increased grip strength J:211773
increased heart rate variability J:211773
thick ventricular wall J:211773
Lsm1tm1b(EUCOMM)Hmgu/Lsm1tm1b(EUCOMM)Hmgu
C57BL/6N-Lsm1tm1b(EUCOMM)Hmgu/Ieg
abnormal auditory brainstem response J:211773
abnormal lens morphology J:211773
cataract J:211773
decreased grip strength J:211773
decreased locomotor activity J:211773
dilated aorta J:211773
hyperactivity J:211773
increased circulating alkaline phosphatase level J:211773
increased heart rate variability J:211773
increased mean corpuscular volume J:211773
preweaning lethality, incomplete penetrance J:211773
prolonged RR interval J:211773

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