PKHD1 Gene Set

Dataset Pathway Commons Protein-Protein Interactions
Category physical interactions
Type interacting protein
Description polycystic kidney and hepatic disease 1 (autosomal recessive)|The protein encoded by this gene is predicted to have a single transmembrane (TM)-spanning domain and multiple copies of an immunoglobulin-like plexin-transcription-factor domain. Alternative splicing results in two transcript variants encoding different isoforms. Other alternatively spliced transcripts have been described, but the full length sequences have not been determined. Several of these transcripts are predicted to encode truncated products which lack the TM and may be secreted. Mutations in this gene cause autosomal recessive polycystic kidney disease, also known as polycystic kidney and hepatic disease-1. [provided by RefSeq, Jul 2008] (NCBI Entrez Gene Database, 5314)
External Link http://www.ncbi.nlm.nih.gov/gene/5314
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Genes

2 interacting proteins for PKHD1 from the Pathway Commons Protein-Protein Interactions dataset.

Symbol Name
CAMLG calcium modulating ligand
LGR4 leucine-rich repeat containing G protein-coupled receptor 4