wdpcp Phenotypes

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Phenotypes

Gene Literature (8)

Nucleotides (85)

Interactants (131)

XB-GENEPAGE-5820823

Gene Symbol: wdpcp Gene Name: WD repeat containing planar cell polarity effector

Monarch Ortholog Phenotypes These phenotypes are associated with this gene with a has phenotype relation via Monarch.
Human (35 sources): 2-3 finger syndactyly, Abnormal electroretinogram, Benign neoplasm of the central nervous system, Broad hallux, Coarctation of aorta, Complete atrioventricular canal defect, Cryptorchidism, Downslanted palpebral fissures, Eczema, Finger syndactyly, Generalized hirsutism, Hamartoma of tongue, Hearing impairment, Hepatic fibrosis, Hypertelorism, Hypertension, Hypogonadism, Hypoplasia of penis, Hypoplasia of the ovary, Intellectual disability, Low-set, posteriorly rotated ears, Medial flaring of the eyebrow, Multicystic kidney dysplasia, Nephrotic syndrome, Neurological speech impairment, Nystagmus, Obesity, Patent ductus arteriosus, Pigmentary retinopathy, Postaxial hand polydactyly, Prominent nasal bridge, Short neck, Short stature, Skeletal muscle atrophy, Subvalvular aortic stenosis [+]
Mouse (17 sources): abnormal cardiac outflow tract development, abnormal cell morphology, abnormal cochlear hair cell morphology, abnormal embryonic neuroepithelium morphology, abnormal heart development, abnormal kidney collecting duct morphology, abnormal kinocilium morphology, abnormal podocyte motility, abnormal septation of the cloaca, abnormal truncus arteriosus septation, atrioventricular septal defect, duplex kidney, embryo phenotype, impaired fibroblast cell migration, perinatal lethality, complete penetrance, renal glomerulus cyst, respiratory system phenotype [+]
View all ortholog results at Monarch