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Symbol Name ID |
Cers3
ceramide synthase 3 MGI:2681008 |
| Darker colors indicate more annotations |
| Human Phenotypes | Palmar hyperlinearity |
Erythroderma |
Hypohidrosis |
Epidermal acanthosis |
Hypergranulosis |
Hyperkeratosis |
Congenital nonbullous ichthyosiform erythroderma |
Orthokeratosis |
| Disease(s) Associated with CERS3 | ||||||||
| autosomal recessive congenital ichthyosis 9 |
| Mouse Phenotypes | impaired skin barrier function |
abnormal stratum corneum lipid matrix formation |
hyperkeratosis |
impaired stratum corneum desquamation |
abnormal epidermal lamellar body morphology |
abnormal skin appearance |
reddish skin |
abnormal skin development |
abnormal keratinocyte physiology |
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| Availability | Mouse Genotype | |||||||||
| Cers3tm1.1Rsnd/Cers3tm1.1Rsnd | ||||||||||
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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last database update 04/16/2024 MGI 6.23 |
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