rap1b Phenotypes

XB-GENEPAGE-479035

Gene Symbol: rap1b Gene Name: RAP1B, member of RAS oncogene family

Monarch Ortholog Phenotypes These phenotypes are associated with this gene with a has phenotype relation via Monarch.
Human (63 sources): Abnormal cardiac septum morphology, Abnormal dermatoglyphics, Abnormal form of the vertebral bodies, Abnormal localization of kidney, Abnormality of dental morphology, Abnormality of immune system physiology, Abnormality of the dentition, Blue sclerae, Butterfly vertebrae, Cerebral cortical atrophy, Cleft palate, Coarctation of aorta, Coloboma, Conductive hearing impairment, Congenital diaphragmatic hernia, Crossed fused renal ectopia, Cryptorchidism, Duplicated collecting system, EEG abnormality, Eversion of lateral third of lower eyelids, Failure to thrive, Feeding difficulties, Hemivertebrae, High palate, Highly arched eyebrow, Hip dislocation, Hydrocephalus, Hydronephrosis, Hypodontia, Hypoplasia of penis, Hypospadias, Hypotonia, Lip pit, Long eyelashes, Macrotia, Mask-like facies, Microcephaly, Microcornea, Microdontia, Nystagmus, Obesity, Orofacial cleft, Preauricular skin tag, Precocious puberty, Protruding ear, Ptosis, Recurrent infections, Renal hypoplasia/aplasia, Scoliosis, Seizure, Sensorineural hearing impairment, Short 5th finger, Short columella, Short middle phalanx of finger, Short stature, Small hand, Sparse lateral eyebrow, Strabismus, Ureteropelvic junction obstruction, Ventriculomegaly, Vertebral clefting, Widely spaced teeth, obsolete Joint hyperflexibility [+]
Mouse (6 sources): decreased body size, decreased litter size, decreased susceptibility to induced thrombosis, lethality throughout fetal growth and development, incomplete penetrance, perinatal lethality, incomplete penetrance, postnatal lethality, incomplete penetrance
View all ortholog results at Monarch