cyp7b1 Phenotypes

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Phenotypes

Gene Literature (0)

Nucleotides (67)

Interactants (2)

XB-GENEPAGE-5896976

Gene Symbol: cyp7b1 Gene Name: cytochrome P450 family 7 subfamily B member 1

Monarch Ortholog Phenotypes These phenotypes are associated with this gene with a has phenotype relation via Monarch.
Human (54 sources): Abnormal cerebellum morphology, Abnormal cerebral white matter morphology, Abnormality of coagulation, Abnormality of the coagulation cascade, Abnormality of the urinary system, Acholic stools, Ankle clonus, Atrophy of the spinal cord, Babinski sign, Biliary tract abnormality, Cataract, Cirrhosis, Cognitive impairment, Congenital hepatic fibrosis, Diarrhea, Dysarthria, Dysphagia, Elevated circulating alkaline phosphatase concentration, Elevated circulating hepatic transaminase concentration, Failure to thrive, Gastrointestinal hemorrhage, Hepatic failure, Hepatitis, Hepatomegaly, Hyperintensity of cerebral white matter on MRI, Hyperreflexia, Impaired distal proprioception, Impaired vibration sensation in the lower limbs, Impaired vibratory sensation, Intrahepatic cholestasis, Jaundice, Limb ataxia, Limb dysmetria, Lower limb amyotrophy, Lower limb muscle weakness, Lower limb spasticity, Neonatal cholestatic liver disease, Nystagmus, Optic atrophy, Paraplegia, Pes cavus, Polyneuropathy, Pruritus, Scoliosis, Sensorineural hearing impairment, Spastic gait, Spastic paraplegia, Splenomegaly, Steatorrhea, Truncal ataxia, Upper limb amyotrophy, Upper limb muscle weakness, Upper limb spasticity, Urinary incontinence [+]
Mouse (7 sources): abnormal estrous cycle, abnormal mammary gland development, abnormal uterus development, absent estrous cycle, homeostasis/metabolism phenotype, premature ovarian failure, uterus atrophy
View all ortholog results at Monarch