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Symbol
Name
ID

Lrsam1
leucine rich repeat and sterile alpha motif containing 1
MGI:2684789

Phenotype annotations related to nervous system

Darker colors indicate more annotations

Human Phenotypes	Peripheral axonal degeneration	Axonal degeneration	Axonal degeneration/regeneration	Fasciculations	Decreased motor nerve conduction velocity	Areflexia	Hyporeflexia	Steppage gait	Tip-toe gait	Distal sensory impairment	Impaired distal vibration sensation
Disease(s) Associated with LRSAM1
Charcot-Marie-Tooth disease axonal type 2P

Mouse Phenotypes		abnormal axon morphology	abnormal neuromuscular synapse morphology	axon degeneration	decreased nerve conduction velocity	decreased prepulse inhibition
Availability	Mouse Genotype	abnormal axon morphology	abnormal neuromuscular synapse morphology	axon degeneration	decreased nerve conduction velocity	decreased prepulse inhibition
	Lrsam1^em1(IMPC)Bay/Lrsam1^em1(IMPC)Bay
	Lrsam1^{Gt(RRK461)Byg}/Lrsam1^{Gt(RRK461)Byg}
	Lrsam1^{Gt(RRK461)Byg}/Lrsam1⁺

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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