cib2 Phenotypes

Phenotypes

XB-GENEPAGE-985355

Gene Symbol: cib2 Gene Name: calcium and integrin binding family member 2

Monarch Ortholog Phenotypes These phenotypes are associated with this gene with a has phenotype relation via Monarch.
Human (28 sources): Abnormal cochlea morphology, Abnormal dental enamel morphology, Abnormal electroretinogram, Abnormal vestibular function, Absent vestibular function, Anxiety, Aplasia/Hypoplasia of the cerebellum, Ataxia, Cataract, Cerebral cortical atrophy, Depression, Global developmental delay, Hallucinations, Hemianopia, High hypermetropia, Intellectual disability, Iris hypopigmentation, Motor delay, Nyctalopia, Profound sensorineural hearing impairment, Rod-cone dystrophy, Schizophrenia, Scotoma, Sensorineural hearing impairment, Subcortical cerebral atrophy, Undetectable electroretinogram, Vestibular hyporeflexia, Visual loss [+]
Mouse (15 sources): abnormal circulating cholesterol level, abnormal cochlear hair cell morphology, abnormal ear morphology, abnormal hair cell mechanoelectric transduction, abnormal hearing physiology, abnormal startle reflex, absent cochlear microphonics, absent distortion product otoacoustic emissions, cochlear hair cell degeneration, deafness, decreased prepulse inhibition, decreased startle reflex, increased or absent threshold for auditory brainstem response, limb grasping, vision/eye phenotype [+]
View all ortholog results at Monarch