External Ids for PXN Gene
This gene encodes a cytoskeletal protein involved in actin-membrane attachment at sites of cell adhesion to the extracellular matrix (focal adhesion). Alternatively spliced transcript variants encoding different isoforms have been described for this gene. These isoforms exhibit different expression pattern, and have different biochemical, as well as physiological properties (PMID:9054445). [provided by RefSeq, Aug 2011]
GeneCards Summary for PXN Gene
PXN (Paxillin) is a Protein Coding gene. Diseases associated with PXN include corneal opacification and other ocular anomalies. Among its related pathways are PI-3K cascade and Signaling by FGFR. GO annotations related to this gene include protein kinase binding and beta-catenin binding. An important paralog of this gene is LDB3.
UniProtKB/Swiss-Prot for PXN Gene
Cytoskeletal protein involved in actin-membrane attachment at sites of cell adhesion to the extracellular matrix (focal adhesion)