abnormal circulating interleukin-12b level Gene Set

Dataset	MPO Gene-Phenotype Associations
Category	disease or phenotype associations
Type	phenotype
Description	anomaly in the amount in the blood of the p40 cytokine subunit that is a component of both interleukin-12 and interleukin-23 (Mammalian Phenotype Ontology, MP_0008646)
External Link	http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0008646
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Genes

15 gene mutations causing the abnormal circulating interleukin-12b level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol	Name
IFIT2	interferon-induced protein with tetratricopeptide repeats 2
IL10	interleukin 10
IL22	interleukin 22
IL27	interleukin 27
IRF5	interferon regulatory factor 5
MYD88	myeloid differentiation primary response 88
NFIL3	nuclear factor, interleukin 3 regulated
NLRP3	NLR family, pyrin domain containing 3
PELI1	pellino E3 ubiquitin protein ligase 1
SLAMF6	SLAM family member 6
STAT1	signal transducer and activator of transcription 1, 91kDa
TICAM1	toll-like receptor adaptor molecule 1
TNFRSF10A	tumor necrosis factor receptor superfamily, member 10a
TRPM2	transient receptor potential cation channel, subfamily M, member 2
UNC93B1	unc-93 homolog B1 (C. elegans)