wdr19 Phenotypes

Click here to close Hello! We notice that you are using Internet Explorer, which is not supported by Xenbase and may cause the site to display incorrectly. We suggest using a current version of Chrome, FireFox, or Safari.

Phenotypes

Gene Literature (3)

Nucleotides (94)

Interactants (121)

XB-GENEPAGE-920012

Gene Symbol: wdr19 Gene Name: WD repeat domain 19

Monarch Ortholog Phenotypes These phenotypes are associated with this gene with a has phenotype relation via Monarch.
Human (81 sources): Abnormal clavicle morphology, Abnormal dental enamel morphology, Abnormal diaphysis morphology, Abnormal fingernail morphology, Abnormal rib morphology, Abnormal sternum morphology, Abnormal toenail morphology, Abnormality of bone mineral density, Abnormality of pelvic girdle bone morphology, Abnormality of retinal pigmentation, Abnormality of the dentition, Abnormality of the liver, Abnormality of the metaphysis, Anemia, Anteverted nares, Aplasia/Hypoplasia of the lungs, Ataxia, Brachydactyly, Cataract, Chronic kidney disease, Clinodactyly of the 5th finger, Cone-shaped epiphysis, Congenital hepatic fibrosis, Craniosynostosis, Dolichocephaly, Epicanthus, Everted lower lip vermilion, Feeding difficulties in infancy, Finger syndactyly, Frontal bossing, Global developmental delay, Growth delay, Hepatic cysts, High hypermetropia, Hypertension, Hypodontia, Hyposthenuria, Hypotelorism, Macular atrophy, Microdontia, Micromelia, Mild proteinuria, Myopia, Narrow chest, Nephronophthisis, Nephropathy, Nystagmus, Osteoporosis, Pallor, Pancreatic cysts, Pectus excavatum, Polydactyly, Polydipsia, Polyuria, Postaxial foot polydactyly, Postaxial hand polydactyly, Premature ovarian insufficiency, Progressive visual loss, Prominent occiput, Reduced visual acuity, Renal corticomedullary cysts, Renal hypoplasia, Renal insufficiency, Renal tubular atrophy, Respiratory insufficiency, Retinal dystrophy, Rhizomelia, Short distal phalanx of finger, Short foot, Short stature, Short thorax, Skeletal dysplasia, Sparse hair, Stage 5 chronic kidney disease, Taurodontia, Toe syndactyly, Tubular basement membrane disintegration, Tubulointerstitial fibrosis, Vascular dilatation, Visual impairment, obsolete Joint hyperflexibility [+]
Mouse (28 sources): abnormal cell morphology, abnormal craniofacial development, abnormal cranium morphology, abnormal dermomyotome development, abnormal limb development, abnormal limb mesenchyme morphology, abnormal limb paddle morphology, abnormal mandibular angle morphology, abnormal maxilla morphology, abnormal myotome development, abnormal palatal shelf fusion at midline, abnormal palatine bone morphology, abnormal somite development, abnormal spine curvature, abnormal sternum ossification, abnormal tympanic ring morphology, absent frontal bone, absent supraoccipital bone, decreased palatine bone horizontal plate size, ectopic digits, embryonic lethality during organogenesis, complete penetrance, interparietal bone hypoplasia, lethality throughout fetal growth and development, complete penetrance, parietal bone hypoplasia, polyphalangy, short mandible, short maxilla, short premaxilla [+]
View all ortholog results at Monarch