| Summary: | Intrahepatic cholestasis is characterized by the accumulation of compounds in the serum that are normally secreted by hepatocytes into the bile. Genes associated with familial intrahepatic cholestasis (FIC) include <i>ATP8B1</i> (FIC1), <i>ABCB11</i> (FIC2), <i>ABCB4</i> (FIC3), <i>TJP2</i> (FIC4), <i>NR1H4</i> (FIC5) and <i>MYO5B</i> (FIC6). With advanced genome sequencing methodologies, additional mutated genes are rapidly identified in patients presenting with idiopathic FIC. Notably, several of these genes, <i>VPS33B</i>, <i>VIPAS39</i>, <i>SCYL1</i>, and <i>AP1S1</i>, together with <i>MYO5B</i>, are functionally associated with recycling endosomes and/or the Golgi apparatus. These are components of a complex process that controls the sorting and trafficking of proteins, including those involved in bile secretion. These gene variants therefore suggest that defects in intracellular trafficking take a prominent place in FIC. Here we review these FIC-associated trafficking genes and their variants, their contribution to biliary transporter and canalicular protein trafficking, and, when perturbed, to cholestatic liver disease. Published variants for each of these genes have been summarized in table format, providing a convenient reference for those who work in the intrahepatic cholestasis field.
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