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Symbol
Name
ID

Mtmr2
myotubularin related protein 2
MGI:1924366

Phenotype annotations related to nervous system

*	Aspects of the system are reported to show a normal phenotype.
	Darker colors indicate more annotations

Human Phenotypes	Facial palsy	Irregular myelin loops	Myelin outfoldings	Abnormal auditory evoked potentials	Decreased motor nerve conduction velocity	Motor delay	Distal sensory impairment
Disease(s) Associated with MTMR2
Charcot-Marie-Tooth disease type 4B1

Mouse Phenotypes		nervous system phenotype	abnormal sciatic nerve morphology	axon degeneration	abnormal myelination	abnormal nerve conduction
Availability	Mouse Genotype	nervous system phenotype	abnormal sciatic nerve morphology	axon degeneration	abnormal myelination	abnormal nerve conduction
	Mtmr2^tm1.1Abol/Mtmr2^tm1.1Abol
	Mtmr2^tm1Ueli/Mtmr2^tm1Ueli	*
	Mtmr2^tm1Abol/Mtmr2^tm1Abol Tg(Mpz-cre)26Mes/0 (conditional)

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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