cyp7a1 Phenotypes

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Phenotypes

Gene Literature (1)

Nucleotides (51)

Interactants (3)

XB-GENEPAGE-485169

Gene Symbol: cyp7a1 Gene Name: cytochrome P450 family 7 subfamily A member 1

Monarch Ortholog Phenotypes These phenotypes are associated with this gene with a has phenotype relation via Monarch.
Human (15 sources): Abnormality of vitamin A metabolism, Abnormality of vitamin E metabolism, Accelerated atherosclerosis, Acute hepatic steatosis, Aortic atherosclerotic lesion, Cholestasis, Cholesterol gallstones, Coronary artery atherosclerosis, Hepatic steatosis, Hepatitis, Hypercholesterolemia, Hypertriglyceridemia, Increased LDL cholesterol concentration, Macrovesicular hepatic steatosis, Obesity [+]
Mouse (34 sources): abnormal bile composition, abnormal bile salt homeostasis, abnormal bile salt level, abnormal blood urea nitrogen level, abnormal circulating alkaline phosphatase level, abnormal circulating amylase level, abnormal circulating cholesterol level, abnormal circulating iron level, abnormal epidermis stratum basale morphology, abnormal epidermis stratum granulosum morphology, abnormal fat-soluble vitamin level, abnormal lipid homeostasis, abnormal retina vasculature morphology, abnormal skin condition, abnormal startle reflex, decreased birth weight, decreased blood urea nitrogen level, decreased circulating iron level, decreased exploration in new environment, decreased intestinal cholesterol absorption, decreased locomotor activity, decreased mean corpuscular volume, delayed eyelid opening, flaky skin, greasy coat, increased circulating alkaline phosphatase level, increased circulating amylase level, increased circulating unsaturated transferrin level, increased startle reflex, oily skin, perinatal lethality, incomplete penetrance, postnatal lethality, incomplete penetrance, thin dermal layer, thin epidermis stratum spinosum [+]
View all ortholog results at Monarch