rev3l Phenotypes

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Phenotypes

Gene Literature (1)

Nucleotides (137)

Interactants (9)

XB-GENEPAGE-1012629

Gene Symbol: rev3l Gene Name: REV3 like, DNA directed polymerase zeta catalytic subunit

Monarch Ortholog Phenotypes These phenotypes are associated with this gene with a has phenotype relation via Monarch.
Human (79 sources): Abducens palsy, Abnormal nasopharynx morphology, Abnormal pinna morphology, Abnormal posterior cranial fossa morphology, Abnormality of pelvic girdle bone morphology, Abnormality of the dentition, Abnormality of the nail, Abnormality of the sense of smell, Abnormality of the ulna, Abnormality of the voice, Absent hand, Aplasia of the pectoralis major muscle, Aplasia/Hypoplasia involving the metacarpal bones, Aplasia/Hypoplasia of the radius, Aplasia/Hypoplasia of the thumb, Aplasia/Hypoplasia of the tongue, Arthrogryposis multiplex congenita, Autism, Bifid uvula, Blepharitis, Brachydactyly, Breast aplasia, Camptodactyly, Cleft palate, Clinodactyly, Clinodactyly of the 5th finger, Clumsiness, Congenital fibrosis of extraocular muscles, Corneal opacity, Cranial nerve paralysis, Decreased testicular size, Delayed speech and language development, Depressed nasal bridge, Dysarthria, Dysdiadochokinesis, Dysphagia, Epicanthus, Esotropia, Everted lower lip vermilion, Exotropia, Facial diplegia, Facial palsy, Feeding difficulties in infancy, Finger syndactyly, Gait disturbance, Hand clenching, Hearing impairment, High palate, Hypertelorism, Hypogonadotropic hypogonadism, Hypoplasia of the brainstem, Hypotonia, Infantile muscular hypotonia, Intellectual disability, mild, Lower limb undergrowth, Mask-like facies, Microdontia, Micrognathia, Micropenis, Microphthalmia, Motor delay, Multiple cafe-au-lait spots, Open mouth, Ophthalmoplegia, Peripheral neuropathy, Pes planus, Poor coordination, Ptosis, Radial deviation of finger, Respiratory distress, Short neck, Short phalanx of finger, Skeletal muscle atrophy, Split hand, Strabismus, Syndactyly, Talipes equinovarus, Tooth agenesis, Visual impairment [+]
Mouse (27 sources): abnormal class switch recombination, abnormal craniofacial development, abnormal embryonic neuroepithelium morphology, abnormal embryonic tissue morphology, abnormal mesenchyme morphology, abnormal somatic hypermutation frequency, abnormal somite shape, abnormal visceral yolk sac morphology, abnormal vitelline vasculature morphology, decreased B cell proliferation, decreased IgG1 level, decreased embryo size, decreased germinal center B cell number, delayed embryo turning, embryonic growth arrest, embryonic growth retardation, embryonic lethality between implantation and somite formation, complete penetrance, embryonic lethality during organogenesis, complete penetrance, immune system phenotype, incomplete somite formation, increased cell death, increased embryonic tissue cell apoptosis, increased mammary gland tumor incidence, neural tube degeneration, pericardial edema, preweaning lethality, complete penetrance, spontaneous chromosome breakage [+]
View all ortholog results at Monarch