Monarch Ortholog Phenotypes
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Human (13 sources):
Anhidrosis,
Anhidrotic ectodermal dysplasia,
Aplasia of the sweat glands,
Concave nasal ridge,
Conical tooth,
Defective production of NFKB1-dependent cytokines,
Frontal bossing,
Heat intolerance,
Hypodontia,
Hypohidrosis,
[+]
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Mouse (67 sources):
abnormal cell differentiation,
abnormal circulating cytokine level,
abnormal epidermis stratum basale morphology,
abnormal epidermis stratum corneum morphology,
abnormal epidermis stratum granulosum morphology,
abnormal erythropoiesis,
abnormal granulocyte differentiation,
abnormal humoral immune response,
abnormal keratinocyte morphology,
abnormal macrophage physiology,
abnormal marginal zone B cell morphology,
abnormal myelopoiesis,
abnormal skin condition,
abnormal T cell activation,
abnormal tumor necrosis factor level,
absent spleen germinal center,
acanthosis,
autoimmune response,
chronic inflammation,
decreased B-2 B cell number,
decreased B cell proliferation,
decreased body size,
decreased CD4-positive, alpha-beta memory T cell number,
decreased CD4-positive, alpha beta T cell number,
decreased double-negative T cell number,
decreased double-positive T cell number,
decreased follicular B cell number,
decreased IgG1 level,
decreased IgG2b level,
decreased marginal zone B cell number,
decreased mature B cell number,
decreased Peyer's patch number,
decreased regulatory T cell number,
decreased T cell proliferation,
decreased thymocyte number,
decreased transitional stage T2 B cell number,
dermatitis,
flaky skin,
hematopoietic system phenotype,
increased activated T cell number,
increased activation-induced B cell apoptosis,
increased anti-insulin autoantibody level,
increased anti-nuclear antigen antibody level,
increased B cell proliferation,
increased bone marrow cell number,
increased circulating interleukin-17 level,
increased circulating interleukin-1 alpha level,
increased circulating tumor necrosis factor level,
increased double-positive T cell number,
increased granulocyte number,
increased immature B cell number,
increased macrophage cell number,
increased memory T cell number,
increased pre-B cell number,
increased pro-B cell number,
increased single-positive T cell number,
increased susceptibility to bacterial infection induced morbidity/mortality,
increased T cell apoptosis,
increased T cell proliferation,
increased thymocyte number,
no abnormal phenotype detected,
postnatal lethality, complete penetrance,
premature death,
small Peyer's patches,
small spleen,
spleen atrophy,
thymus atrophy
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View all ortholog results at Monarch
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