cyp4f22 Phenotypes

Phenotypes

XB-GENEPAGE-5889577

Gene Symbol: cyp4f22 Gene Name: cytochrome P450 family 4 subfamily F member 22

Expression Phenotypes Gene expression phenotype annotations where the gene of interest has been disrupted (manipulated) or is the gene assayed (assayed). Computed annotations are derived from differential expression analysis from Xenbase processed GEO data with the criteria of a TPM >= 1, FDR <= 0.05 and an absolute LogFC >= 2.
Computed annotations: cyp4f22 assayed (1 source)

Monarch Ortholog Phenotypes These phenotypes are associated with this gene with a has phenotype relation via Monarch.
Human (28 sources): Abnormal helix morphology, Abnormality of the dentition, Abnormality of the nail, Acanthocytosis, Aplasia/Hypoplasia of the eyebrow, Chronic otitis media, Cognitive impairment, Congenital nonbullous ichthyosiform erythroderma, Dehydration, Dry skin, Ectropion, Epidermal acanthosis, Erythroderma, Everted lower lip vermilion, Gangrene, Hyperkeratosis, Ichthyosis, Lack of skin elasticity, Orthokeratosis, Palmoplantar keratoderma, Parakeratosis, Pruritus, Recurrent respiratory infections, Renal insufficiency, Sepsis, Short stature, Sparse hair, obsolete Hypotrichosis [+]
View all ortholog results at Monarch

Monarch Ortholog Phenotypes

These phenotypes are associated with this gene with a has phenotype relation via Monarch.

Human (28 sources): Abnormal helix morphology, Abnormality of the dentition, Abnormality of the nail, Acanthocytosis, Aplasia/Hypoplasia of the eyebrow, Chronic otitis media, Cognitive impairment, Congenital nonbullous ichthyosiform erythroderma, Dehydration, Dry skin, [+]