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Symbol
Name
ID
Plec
plectin
MGI:1277961
Phenotype annotations related to behavior/neurological
*Aspects of the system are reported to show a normal phenotype.
Darker colors indicate more annotations
Human Phenotypes
Hypernasal speech
Fatigue
Disease(s) Associated with PLEC
autosomal recessive limb-girdle muscular dystrophy type 2Q
epidermolysis bullosa simplex with muscular dystrophy

Mouse Phenotypes
behavior/neurological phenotype
abnormal suckling behavior
impaired exercise endurance
Availability Mouse Genotype
Plec/Parp10tm1.1Gwi/Plec/Parp10tm1.1Gwi *
Plectm4Gwi/Plectm4Gwi
Tg(KRT5-cre)1Tak/?  (conditional)
Plectm4Gwi/Plectm4Gwi
Tg(Ckmm-cre)5Khn/?  (conditional)
Plectm1Gwi/Plectm4Gwi
Tg(Ckmm-cre)5Khn/?  (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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last database update
04/16/2024
MGI 6.23
The Jackson Laboratory