abnormal circulating serum amyloid protein level Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description deviation from the normal blood levels of an acute-phase reaction protein that is a precursor to amyloid A protein; it is present in very high levels during acute inflammatory episodes, and is present in low concentrations in normal sera, but is found at higher concentrations in sera of older persons and in patients with amyloidosis (Mammalian Phenotype Ontology, MP_0010214)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0010214
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8 gene mutations causing the abnormal circulating serum amyloid protein level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
CREB3L3 cAMP responsive element binding protein 3-like 3
GPR21 G protein-coupled receptor 21
IL1R1 interleukin 1 receptor, type I
IL1RN interleukin 1 receptor antagonist
IL6R interleukin 6 receptor
LIF leukemia inhibitory factor
PTGER4 prostaglandin E receptor 4 (subtype EP4)
PTPN6 protein tyrosine phosphatase, non-receptor type 6