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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID 		Nrcam
neuronal cell adhesion molecule
MGI:104750
38 phenotypes from multigenic genotypes
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Allelic Composition
Genetic Background		 Annotated Term Reference
Cntnap1tm1Pele/Cntnap1tm1Pele
Nrcamtm1Gmt/Nrcamtm1Gmt
involves: 129P2/OlaHsd * ICR 		abnormal axon morphology J:166099
ataxia J:166099
decreased nerve conduction velocity J:166099
paralysis J:166099
postnatal lethality, complete penetrance J:166099
Gars1C201R/Gars1+
Nrcamm1J/Nrcamm1J
involves: BALB/cAnN * C3H/HeH * C57BL/6J 		abnormal axon morphology J:240096
abnormal innervation pattern to muscle J:240096
abnormal neuromuscular synapse morphology J:240096
decreased nerve conduction velocity J:240096
impaired coordination J:240096
muscle hypoplasia J:240096
tremors J:240096
L1camtm1Sor/L1cam+
Nrcamtm1Gmt/Nrcamtm1Gmt
involves: 129S6/SvEvTac * 129S7/SvEvBrd * Swiss Webster 		postnatal lethality, incomplete penetrance J:71828
L1camtm1Sor/Y
Nrcamtm1Gmt/Nrcam+
involves: 129S6/SvEvTac * 129S7/SvEvBrd * Swiss Webster 		postnatal lethality, incomplete penetrance J:71828
L1camtm1Sor/Y
Nrcamtm1Gmt/Nrcamtm1Gmt
involves: 129S6/SvEvTac * 129S7/SvEvBrd * Swiss Webster 		abnormal cerebellar cortex morphology J:71828
abnormal cerebellar foliation J:71828
abnormal cerebellar granule layer morphology J:71828
abnormal cerebellum development J:71828
abnormal cerebellum external granule cell layer morphology J:71828
decreased body weight J:71828
postnatal lethality J:71828
small cerebellum J:71828
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/Lpin1fld
Nrcam20884/Nrcam20884
involves: BALB/cByJ * C57BL/6J 		forelimb paresis J:153042
hindlimb paralysis J:153042
postnatal growth retardation J:153042
skeletal muscle fiber atrophy J:153042
Nfasctm1.1Brp/Nfasctm1.1Brp
Nrcamtm1Gmt/Nrcamtm1Gmt
involves: 129P2/OlaHsd * 129S6/SvEvTac * ICR 		abnormal axon morphology J:166099
Nrcamm1J/Nrcamm1J
Sh3tc2m1J/Sh3tc2m1J
B6.Cg-Nrcamm1J Sh3tc2m1J/GrsrRwb 		abnormal nerve conduction J:240096
abnormal neuromuscular synapse morphology J:240096
decreased nerve conduction velocity J:240096
heart block J:240096
muscular atrophy J:240096
paralysis J:240096
premature death J:240096
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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Send questions and comments to User Support. 		last database update
04/16/2024
MGI 6.23 		The Jackson Laboratory