The following gene names and symbols are associated with antigen Polycystic Kidney Disease 1 (Autosomal Dominant) across different species:

polycystic kidney disease 1 (autosomal dominant) (PKD1), polycystic kidney disease 1 homolog (Pkd1), polycystic kidney disease 1 homolog (human) (Pkd1)

Other aliases include:

PBP, Pc-1, PC1, FLJ00285, MGC118471, mFLJ00285

On the protein level the following designations are being used for antigen Polycystic Kidney Disease 1 (Autosomal Dominant):

polycystin 1 – polycystic kidney disease-associated protein – polycystin-1 – polycystic kidney disease 1 homolog; polycystin-1 – autosomal dominant polycystic kidney disease 1 protein homolog – polycystic kidney disease 1 (autosomal dominant)

Polycystic Kidney Disease 1 (Autosomal Dominant) fulfills a number of functions:

protein binding – sugar binding – binding – calcium channel activity – cation channel activity – molecular_function

Polycystic Kidney Disease 1 (Autosomal Dominant) is relevant to the following processes:

anatomical structure morphogenesis – calcium-independent cell-matrix adhesion – homophilic cell adhesion – neuropeptide signaling pathway – JAK-STAT cascade – blood vessel development – calcium ion transmembrane transport – calcium ion transport – cartilage condensation – cation transport – cell cycle arrest – cell-cell adhesion – detection of mechanical stimulus – heart development – in utero embryonic development – ion transmembrane transport – biological_process

Locations for Polycystic Kidney Disease 1 (Autosomal Dominant):

integral to plasma membrane – membrane – Golgi apparatus – cilium – integral to membrane – lateral plasma membrane – membrane fraction – motile primary cilium – nucleus – plasma membrane – polycystin complex

Source: NCBI Entrez Gene, Gene Ontology