cngb1 Phenotypes

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Phenotypes

Gene Literature (19)

Nucleotides (52)

Interactants (43)

XB-GENEPAGE-980341

Gene Symbol: cngb1 Gene Name: cyclic nucleotide gated channel beta 1

Monarch Ortholog Phenotypes These phenotypes are associated with this gene with a has phenotype relation via Monarch.
Human (33 sources): Abnormal electroretinogram, Abnormal retinal vascular morphology, Abnormal testis morphology, Abnormality of fundus pigmentation, Abnormality of retinal pigmentation, Anteverted nares, Atypical scarring of skin, Blindness, Bone spicule pigmentation of the retina, Cataract, Conductive hearing impairment, Constriction of peripheral visual field, Glaucoma, Hyperinsulinemia, Hyperreflexia, Hypogonadism, Hypoplasia of penis, Intellectual disability, Keratoconus, Macular degeneration, Nyctalopia, Nystagmus, Obesity, Ophthalmoplegia, Optic atrophy, Peripheral visual field loss, Photophobia, Progressive night blindness, Rod-cone dystrophy, Sensorineural hearing impairment, Type II diabetes mellitus, Visual impairment, Wide nasal bridge [+]
Mouse (18 sources): abnormal action potential, abnormal neuron physiology, abnormal retina horizontal cell morphology, abnormal retina pigment epithelium morphology, abnormal retina rod bipolar cell morphology, abnormal retina rod cell morphology, abnormal retina rod cell outer segment morphology, abnormal rod electrophysiology, abnormal single cell response, decreased body size, decreased retina photoreceptor cell number, decreased total retina thickness, growth/size/body region phenotype, postnatal lethality, retina photoreceptor degeneration, taste/olfaction phenotype, thin retina outer nuclear layer, vision/eye phenotype [+]
View all ortholog results at Monarch