bbs7 Phenotypes

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Phenotypes

Gene Literature (0)

Nucleotides (111)

Interactants (58)

XB-GENEPAGE-996060

Gene Symbol: bbs7 Gene Name: Bardet-Biedl syndrome 7

Monarch Ortholog Phenotypes These phenotypes are associated with this gene with a has phenotype relation via Monarch.
Human (28 sources): Abnormal electroretinogram, Cryptorchidism, Downslanted palpebral fissures, External genital hypoplasia, Finger syndactyly, Generalized hirsutism, Hearing impairment, Hepatic fibrosis, Hypertension, Hypogonadism, Hypoplasia of penis, Hypoplasia of the ovary, Intellectual disability, Low-set, posteriorly rotated ears, Medial flaring of the eyebrow, Multicystic kidney dysplasia, Nephrotic syndrome, Neurological speech impairment, Nystagmus, Obesity, Pigmentary retinopathy, Polydactyly, Postaxial hand polydactyly, Prominent nasal bridge, Rod-cone dystrophy, Short neck, Short stature, Skeletal muscle atrophy [+]
Mouse (27 sources): abnormal brain ependyma motile cilium morphology, abnormal cilium morphology, abnormal prepulse inhibition, abnormal sperm axoneme morphology, abnormal sperm flagellum morphology, abnormal sperm principal piece morphology, absent sperm flagellum, cellular phenotype, decreased birth body size, decreased brain ependyma motile cilium length, decreased brain ependyma motile cilium number, decreased striatum size, enlarged lateral ventricles, enlarged third ventricle, increased food intake, increased prepulse inhibition, limbs/digits/tail phenotype, nervous system phenotype, photoreceptor inner segment degeneration, photoreceptor outer segment degeneration, preweaning lethality, incomplete penetrance, renal/urinary system phenotype, retina outer nuclear layer degeneration, small hippocampus, taste/olfaction phenotype, thin cerebral cortex, vision/eye phenotype [+]
View all ortholog results at Monarch