Protein-coding gene in the species Homo sapiens
Not to be confused with the neurotoxin
paxilline.
PXN |
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Available structures |
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PDB | Ortholog search: PDBe RCSB |
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List of PDB id codes |
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2O9V, 2VZD, 2VZG, 2VZI, 3GM1, 3PY7, 3U3F, 4EDN, 1OW6, 1OW7, 1OW8, 3RQE, 3RQF, 3RQG, 4XGZ, 4XH2 |
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Identifiers |
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Aliases | PXN, entrez:5829, paxillin |
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External IDs | OMIM: 602505; MGI: 108295; HomoloGene: 37697; GeneCards: PXN; OMA:PXN - orthologs |
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RNA expression pattern |
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Bgee | Human | Mouse (ortholog) |
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Top expressed in | - granulocyte
- tibial nerve
- left uterine tube
- apex of heart
- gastrocnemius muscle
- canal of the cervix
- muscle layer of sigmoid colon
- upper lobe of left lung
- body of uterus
- transverse colon
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| Top expressed in | - granulocyte
- vestibular membrane of cochlear duct
- internal carotid artery
- external carotid artery
- endothelial cell of lymphatic vessel
- retinal pigment epithelium
- right lung lobe
- left lung
- tibiofemoral joint
- stria vascularis
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| More reference expression data |
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BioGPS | |
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Wikidata |
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Paxillin is a protein that in humans is encoded by the PXN gene. Paxillin is expressed at focal adhesions of non-striated cells and at costameres of striated muscle cells, and it functions to adhere cells to the extracellular matrix. Mutations in PXN as well as abnormal expression of paxillin protein has been implicated in the progression of various cancers.