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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID
Micu1
mitochondrial calcium uptake 1
MGI:2384909
27 phenotypes from 2 alleles in 2 genetic backgrounds
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Allelic Composition
Genetic Background
Annotated Term Reference
Micu1em#Fink/Micu1em#Fink
C57BL/6N-Micu1em#Fink
abnormal brain development J:238984
abnormal cerebellum development J:238984
abnormal mitochondrial morphology J:238984
abnormal mitochondrial physiology J:238984
abnormal muscle physiology J:238984
abnormal Purkinje cell dendrite morphology J:238984
ataxia J:238984
decreased B cell number J:238984
decreased birth body size J:238984
decreased follicular B cell number J:238984
decreased grip strength J:238984
decreased skeletal muscle fiber number J:238984
impaired coordination J:238984
increased B cell apoptosis J:238984
increased circulating lactate level J:238984
oxidative stress J:238984
postnatal lethality, incomplete penetrance J:238984
Micu1tm1bNarl/Micu1+
C57BL/6N-Micu1tm1bNarl/Narl
increased total body fat amount J:211773
long tibia J:211773
Micu1tm1bNarl/Micu1tm1bNarl
C57BL/6N-Micu1tm1bNarl/Narl
abnormal gait J:211773
abnormal locomotor behavior J:211773
abnormal snout morphology J:211773
abnormal tail length J:211773
enlarged spleen J:211773
enlarged testis J:211773
preweaning lethality, incomplete penetrance J:211773
small seminal vesicle 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
04/16/2024
MGI 6.23
The Jackson Laboratory