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Symbol
Name
ID

Cyp4f39
cytochrome P450, family 4, subfamily f, polypeptide 39
MGI:2445210

Phenotype annotations related to integument

Darker colors indicate more annotations

Human Phenotypes	Palmoplantar keratoderma	Palmar hyperlinearity	Erythroderma	Epidermal acanthosis	White scaling skin	Congenital nonbullous ichthyosiform erythroderma	Orthokeratosis	Parakeratosis
Disease(s) Associated with CYP4F22
autosomal recessive congenital ichthyosis 5

Mouse Phenotypes		abnormal corneocyte morphology	abnormal Meibomian gland physiology	impaired skin barrier function	abnormal epidermis stratum corneum morphology	abnormal epidermal lamellar body morphology	reddish skin	shiny skin	wrinkled skin
Availability	Mouse Genotype	abnormal corneocyte morphology	abnormal Meibomian gland physiology	impaired skin barrier function	abnormal epidermis stratum corneum morphology	abnormal epidermal lamellar body morphology	reddish skin	shiny skin	wrinkled skin
	Cyp4f39^em1Akih/Cyp4f39^em1Akih
	Cyp4f39^em1Akih/Cyp4f39^em1Akih Tg(IVL-Cyp4f39)6Akih/0

Contributing Projects: Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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