Symbol Name ID |
Porcn
porcupine O-acyltransferase MGI:1890212 |
* | Aspects of the system are reported to show a normal phenotype. |
Darker colors indicate more annotations |
Human Phenotypes | Abnormal palmar dermatoglyphics |
Hypoplastic nipples |
Supernumerary nipple |
Erythema |
Telangiectasia |
Telangiectasia of the skin |
Patchy alopecia |
Alopecia |
Sparse hair |
Brittle hair |
Abnormality of the nail |
Absent toenail |
Absent fingernail |
Nail dysplasia |
Ridged nail |
Nail dystrophy |
Abnormality of skin pigmentation |
Linear hyperpigmentation |
Reticular hyperpigmentation |
Hypopigmentation of the skin |
Aplasia/Hypoplasia of the skin |
Dermal atrophy |
Focal dermal aplasia/hypoplasia |
Thin skin |
Macule |
Skin nodule |
Subcutaneous nodule |
Papilloma |
Disease(s) Associated with PORCN | ||||||||||||||||||||||||||||
focal dermal hypoplasia |
Mouse Phenotypes | integument phenotype |
abnormal hypodermis fat layer morphology |
dermal cyst |
abnormal hair growth |
alopecia |
hairless |
abnormal hair follicle development |
abnormal skin morphology |
abnormal dermal layer morphology |
thin dermal layer |
thin epidermis |
skin lesions |
skin hypoplasia |
thin skin |
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Availability | Mouse Genotype | ||||||||||||||
Porcntm1.2Vdv/Porcn+ | |||||||||||||||
PorcnGt(CSD256)Byg/Y | |||||||||||||||
Porcntm1.1Lcm/Porcn+ Edil3Tg(Sox2-cre)1Amc/Edil3+ (conditional) |
* | ||||||||||||||
Porcntm1.1Lcm/Porcntm1.2Lcm Tg(Six3-cre)69Frty/0 (conditional) |
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Porcntm1.1Vdv/Porcn+ Tg(EIIa-cre)C5379Lmgd/0 (conditional) |
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Porcntm1.1Vdv/Porcn+ Tg(KRT14-cre)1Efu/0 (conditional) |
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Porcntm1.1Lcm/Y Tg(Msx2-cre)5Rem/0 (conditional) |
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Porcntm1.1Vdv/Y Tg(EIIa-cre)C5379Lmgd/0 (conditional) |
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Porcntm1.1Vdv/Y Tg(KRT14-cre)1Efu/0 (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 03/19/2024 MGI 6.23 |
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