PEX5L
Description
The PEX5L (peroxisomal biogenesis factor 5 like) is a protein-coding gene located on chromosome 3.
PEX5L is an accessory subunit of hyperpolarization-activated cyclic nucleotide-gated (HCN) channels, regulating their cell-surface expression and sensitivity to cyclic nucleotides.
PEX5L is also known as PEX5R, PEX5RP, PXR2, PXR2B, TRIP8b.
Associated Diseases
- childhood disintegrative disorder
- nonpapillary renal cell carcinoma
- absence epilepsy
- major depressive disorder
- schizophrenia
