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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
Decreased motor nerve conduction velocity
Peripheral axonal degeneration
Axonal degeneration
Axonal degeneration/regeneration
Distal sensory impairment
Impaired distal vibration sensation
Areflexia
Hyporeflexia
Steppage gait
Toe walking
Fasciculations
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
Availability Mouse Genotype
Lrsam1Gt(RRK461)Byg/Lrsam1Gt(RRK461)Byg
Lrsam1Gt(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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last database update
01/14/2020
MGI 6.14
The Jackson Laboratory