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Symbol
Name
ID

Alox12b
arachidonate 12-lipoxygenase, 12R type
MGI:1274782

Phenotype annotations related to integument

Darker colors indicate more annotations

Human Phenotypes

Palmoplantar keratoderma

Palmar hyperlinearity

Erythema

Abnormal hair morphology

Alopecia

Small nail

Thin nail

Anhidrosis

Hypohidrosis

Epidermal acanthosis

Hypergranulosis

Hyperkeratosis

Congenital ichthyosiform erythroderma

Congenital nonbullous ichthyosiform erythroderma

Disease(s) Associated with ALOX12B

autosomal recessive congenital ichthyosis 2

Mouse Phenotypes		impaired skin barrier function	abnormal epidermis stratum corneum morphology	abnormal epidermis stratum granulosum morphology	dry skin	reddish skin	scaly skin	shiny skin	abnormal skin condition
Availability	Mouse Genotype	impaired skin barrier function	abnormal epidermis stratum corneum morphology	abnormal epidermis stratum granulosum morphology	dry skin	reddish skin	scaly skin	shiny skin	abnormal skin condition
	Alox12b^mmy/Alox12b^mmy
	Alox12b^tm1.1Krie/Alox12b^tm1.1Krie

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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