Symbol Name ID |
Cyp4f39
cytochrome P450, family 4, subfamily f, polypeptide 39 MGI:2445210 |
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 Meibomian gland physiology |
impaired skin barrier function |
abnormal epidermis stratum corneum morphology |
abnormal corneocyte morphology |
abnormal epidermal lamellar body morphology |
reddish skin |
shiny skin |
wrinkled skin |
|
Availability | Mouse Genotype | ||||||||
Cyp4f39em1Akih/Cyp4f39em1Akih | |||||||||
Cyp4f39em1Akih/Cyp4f39em1Akih Tg(IVL-Cyp4f39)6Akih/0 |
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO) |
||
Citing These Resources Funding Information Warranty Disclaimer, Privacy Notice, Licensing, & Copyright Send questions and comments to User Support. |
last database update 04/16/2024 MGI 6.23 |
|
|