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Symbol
Name
ID

Plec
plectin
MGI:1277961

Phenotype annotations related to nervous system

Darker colors indicate more annotations

Human Phenotypes

Bilateral facial palsy

Dysphagia

Oculomotor nerve palsy

Frequent falls

Fatigable weakness

Echolalia

Aphasia

Mutism

Areflexia

Loss of ambulation

Global developmental delay

Motor delay

Delayed gross motor development

Disease(s) Associated with PLEC

autosomal recessive limb-girdle muscular dystrophy type 2Q

epidermolysis bullosa simplex with muscular dystrophy

Mouse Phenotypes		abnormal axon morphology	decreased nerve conduction velocity
Availability	Mouse Genotype	abnormal axon morphology	decreased nerve conduction velocity
	Plec/Parp10^tm1.1Gwi/Plec/Parp10^tm1.1Gwi
	Plec^tm4Gwi/Plec^tm4.1Gwi Tg(Nes-cre)1Kln/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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