Symbol Name ID |
Plec
plectin MGI:1277961 |
* | 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 |
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Availability | Mouse Genotype | |||
Plec/Parp10tm1.1Gwi/Plec/Parp10tm1.1Gwi | * | |||
Plectm4Gwi/Plectm4Gwi Tg(KRT5-cre)1Tak/? (conditional) |
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Plectm4Gwi/Plectm4Gwi Tg(Ckmm-cre)5Khn/? (conditional) |
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Plectm1Gwi/Plectm4Gwi Tg(Ckmm-cre)5Khn/? (conditional) |
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 |
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