traip Phenotypes

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Phenotypes

Gene Literature (0)

Nucleotides (137)

Interactants (23)

XB-GENEPAGE-922320

Gene Symbol: traip Gene Name: TRAF interacting protein

Monarch Ortholog Phenotypes These phenotypes are associated with this gene with a has phenotype relation via Monarch.
Human (48 sources): Abnormal dental enamel morphology, Abnormal earlobe morphology, Absent earlobe, Agonadism, Ambiguous genitalia, Asthma, Atrial septal defect, Cachexia, Clinodactyly of the 5th finger, Clitoral hypertrophy, Cognitive impairment, Cone-shaped epiphysis, Congenital diaphragmatic hernia, Convex nasal ridge, Craniosynostosis, Decreased fetal movement, Delayed skeletal maturation, Dolichocephaly, Downslanted palpebral fissures, Glaucoma, Global developmental delay, Hip dysplasia, Hypertrichosis, Intellectual disability, Intrauterine growth retardation, Long face, Microcephaly, Micrognathia, Mild global developmental delay, Narrow face, Polyhydramnios, Prematurely aged appearance, Protruding ear, Pulmonary artery hypoplasia, Recurrent respiratory infections, Recurrent urinary tract infections, Sandal gap, Scaphocephaly, Scoliosis, Short stature, Simplified gyral pattern, Small for gestational age, Sparse scalp hair, Talipes equinovarus, Tooth agenesis, Ventricular septal defect, Ventriculomegaly, obsolete Joint hyperflexibility [+]
Mouse (7 sources): abnormal embryonic tissue morphology, absent proamniotic cavity, decreased cell proliferation, decreased embryo size, embryonic growth retardation, embryonic lethality between somite formation and embryo turning, complete penetrance, increased embryonic tissue cell apoptosis
View all ortholog results at Monarch