gorab Phenotypes

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Phenotypes

Gene Literature (0)

Nucleotides (55)

Interactants (62)

XB-GENEPAGE-951258

Gene Symbol: gorab Gene Name: golgin, RAB6-interacting

Monarch Ortholog Phenotypes These phenotypes are associated with this gene with a has phenotype relation via Monarch.
Human (47 sources): Abnormal bone ossification, Abnormal form of the vertebral bodies, Abnormality of epiphysis morphology, Abnormality of the orbital region, Abnormality of vision, Beaking of vertebral bodies, Biconcave vertebral bodies, Camptodactyly, Cutis laxa, Deeply set eye, Delayed speech and language development, Femoral bowing, Global developmental delay, Growth delay, Hernia, Hip dislocation, Hyperextensibility of the finger joints, Hyperextensible skin, Hypoplasia of the maxilla, Hypotonia, Increased susceptibility to fractures, Intellectual disability, Intellectual disability, mild, Irregular vertebral endplates, Kyphoscoliosis, Malar flattening, Mandibular prognathia, Microcephaly, Microcornea, Osteopenia, Osteoporosis, Pectus carinatum, Periodontitis, Pes planus, Platyspondyly, Prematurely aged appearance, Progeroid facial appearance, Recurrent fractures, Redundant skin, Scoliosis, Severe short stature, Talipes equinovarus, Thin skin, Tibial bowing, Vertebral compression fracture, Wormian bones, obsolete Joint hyperflexibility [+]
Mouse (10 sources): abnormal craniofacial morphology, abnormal dermal layer morphology, abnormal dermis papillary layer morphology, abnormal nonmotile primary cilium morphology, decreased hair follicle number, hunched posture, integument phenotype, neonatal lethality, complete penetrance, skin edema, underdeveloped hair follicles
View all ortholog results at Monarch