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