decreased circulating bilirubin level Gene Set

Dataset	MPO Gene-Phenotype Associations
Category	disease or phenotype associations
Type	phenotype
Description	reduced concentration in the blood of the bile pigment bilirubin, normally found in the liver and in red blood cells (Mammalian Phenotype Ontology, MP_0005635)
External Link	http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0005635
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Genes

5 gene mutations causing the decreased circulating bilirubin level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol	Name
BBS5	Bardet-Biedl syndrome 5
CHD7	chromodomain helicase DNA binding protein 7
CMTM6	CKLF-like MARVEL transmembrane domain containing 6
KCNE2	potassium channel, voltage gated subfamily E regulatory beta subunit 2
PIK3C2A	phosphatidylinositol-4-phosphate 3-kinase, catalytic subunit type 2 alpha