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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID
Lpin1
lipin 1
MGI:1891340
20 phenotypes from multigenic genotypes
Export: Excel File
Allelic Composition
Genetic Background
Annotated Term Reference
Lpin120884/Lpin120884
Nrcam20884/Nrcam20884
involves: C57BL/6J
abnormal action potential J:153042
abnormal gait J:153042
abnormal myelin sheath morphology J:153042
abnormal nursing J:153042
abnormal sciatic nerve morphology J:153042
abnormal sexual interaction J:153042
decreased body weight J:153042
decreased grip strength J:153042
decreased joint mobility J:153042
decreased nerve conduction velocity J:153042
demyelination J:153042
hindlimb paralysis J:153042
limb grasping J:153042
paresis J:153042
skeletal muscle fiber atrophy J:153042
Lpin1fld/Lpin1+
Lpin2tm1Reue/Lpin2tm1Reue
involves: BALB/cByJ * C57BL/6J
embryonic growth retardation J:189894
Lpin1fld/Lpin1fld
Lpin2tm1Reue/Lpin2tm1Reue
involves: BALB/cByJ * C57BL/6J
abnormal cardiovascular development J:189894
decreased embryo size J:189894
embryonic lethality during organogenesis, complete penetrance J:189894
Lpin1fld/Lpin1fld
Nrcam20884/Nrcam20884
involves: BALB/cByJ * C57BL/6J
hindlimb paralysis J:153042
paresis J:153042
postnatal growth retardation J:153042
skeletal muscle fiber atrophy J:153042

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
09/10/2019
MGI 6.14
The Jackson Laboratory