mortality/aging
• majority of mice with the acute skin phenotype die within 2 weeks
|
integument
• skin shows inflammatory infiltrates into the epidermis and dermis, including the presence of CD4+ T cells and an increased number of granulocytes and macrophages
• skin hyperproliferation is accompanied by a hematopoietic cell infiltration
|
• hypogranulosis
|
acanthosis
(
J:151886
)
reddish skin
(
J:151886
)
scaly skin
(
J:151886
)
skin lesions
(
J:151886
)
• treatment with etanercept improves skin lesions
|
• mutants develop skin defects resembling psoriasis after P6
• mutants either develop a mild skin phenotype characterized by small scaly patches affecting the ears, tails, paws and hairy back skin or an acute skin phenotype characterized by skin lesions covering the entire body and death within 2 weeks
• the skin defect phenotype is seen as early as 3 days after birth, is most severe at 2 weeks of age and a reversion is seen in surviving mice by 4 weeks
|
thick skin
(
J:151886
)
• inflexible thickened skin
|
growth/size/body
• mice with the acute skin phenotype are runted
|
behavior/neurological
• mice with the acute skin phenotype exhibit decreased feeding activity
|
cellular
homeostasis/metabolism
• some mutants exhibit edema of paws with alteration of nails
|
immune system
• skin shows inflammatory infiltrates into the epidermis and dermis, including the presence of CD4+ T cells and an increased number of granulocytes and macrophages
• skin hyperproliferation is accompanied by a hematopoietic cell infiltration
|
Mouse Models of Human Disease |
DO ID | OMIM ID(s) | Ref(s) | |
psoriasis | DOID:8893 |
OMIM:PS177900 |
J:151886 |