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Symbol
Name
ID
Mpz
myelin protein zero
MGI:103177
Phenotype annotations related to muscle
Darker colors indicate more annotations
Human Phenotypes
Distal lower limb muscle weakness
Limb muscle weakness
Foot dorsiflexor weakness
Upper limb muscle weakness
Hypotonia
Cold-induced muscle cramps
Muscle weakness
Distal muscle weakness
Proximal muscle weakness
Skeletal muscle atrophy
Distal amyotrophy
Skeletal muscle hypertrophy
Disease(s) Associated with MPZ
Charcot-Marie-Tooth disease dominant intermediate D
Charcot-Marie-Tooth disease type 1B
Charcot-Marie-Tooth disease type 2I
Charcot-Marie-Tooth disease type 2J
Charcot-Marie-Tooth disease type 3

Mouse Phenotypes
muscular atrophy
muscle weakness
Availability Mouse Genotype
Tg(Mpz)80.2Wra/0
Tg(Mpz)88.1Mfel/0
Tg(Mpz)88.2Mfel/0
Tg(Mpz)88.4Mfel/0
Tg(Mpz*S63C)32Mes/0
Tg(Mpz*S63C)33Mes/0
Tg(Mpz*S63X)30Mes/0
Tg(Mpz*S63X)31Mes/0

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
04/16/2024
MGI 6.23
The Jackson Laboratory