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Symbol
Name
ID
Aloxe3
arachidonate lipoxygenase 3
MGI:1345140
Phenotype annotations related to integument
Darker colors indicate more annotations
Human Phenotypes
Aplasia/Hypoplasia of the eyebrow
Palmoplantar hyperkeratosis
Palmoplantar keratoderma
Palmar hyperlinearity
Desquamation of skin soon after birth
Erythema
Erythroderma
Alopecia
Sparse hair
Abnormality of the nail
Nail dysplasia
Nail dystrophy
Anhidrosis
Hypohidrosis
Lack of skin elasticity
Epidermal acanthosis
Scaling skin
Dry skin
Thickened skin
Hyperkeratosis
Ichthyosis
Congenital ichthyosiform erythroderma
Congenital nonbullous ichthyosiform erythroderma
Parakeratosis
Pruritus
Disease(s) Associated with ALOXE3
autosomal recessive congenital ichthyosis 1
autosomal recessive congenital ichthyosis 3

Mouse Phenotypes
impaired skin barrier function
abnormal epidermis stratum corneum morphology
hyperkeratosis
impaired stratum corneum desquamation
Availability Mouse Genotype
Aloxe3tm1.2Krie/Aloxe3tm1.2Krie

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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last database update
08/02/2024
MGI 6.24
The Jackson Laboratory