{"@type": "dcat:Dataset", "accessLevel": "public", "bureauCode": ["009:25"], "contactPoint": {"@type": "vcard:Contact", "fn": "NIH", "hasEmail": "mailto:info@nih.gov"}, "description": "Background\n          Receptor protein tyrosine phosphatase rho (RPTP\u03c1, gene symbol PTPRT) is a member of the type IIB RPTP family. These transmembrane molecules have been linked to signal transduction, cell adhesion and neurite extension. The extracellular segment contains MAM, Ig-like and fibronectin type III domains, and the intracellular segment contains two phosphatase domains. The human RPTP\u03c1 gene is located on chromosome 20q12-13.1, and the mouse gene is located on a syntenic region of chromosome 2. RPTP\u03c1 expression is restricted to the central nervous system.\n        \n        \n          Results\n          The cloning of the mouse cDNA, identification of alternatively spliced exons, detection of an 8 kb 3'-UTR, and the genomic organization of human and mouse RPTP\u03c1 genes are described. The two genes are comprised of at least 33 exons. Both RPTP\u03c1 genes span over 1 Mbp and are the largest RPTP genes characterized. Exons encoding the extracellular segment through the intracellular juxtamembrane 'wedge' region are widely spaced, with introns ranging from 9.7 to 303.7 kb. In contrast, exons encoding the two phosphatase domains are more tightly clustered, with 15 exons spanning \u223c 60 kb, and introns ranging in size from 0.6 kb to 13.1 kb. Phase 0 introns predominate in the intracellular, and phase 1 in the extracellular segment.\n        \n        \n          Conclusions\n          We report the first genomic characterization of a RPTP type IIB gene. Alternatively spliced variants may result in different RPTP\u03c1 isoforms. Our findings suggest that RPTP\u03c1 extracellular and intracellular segments originated as separate modular proteins that fused into a single transmembrane molecule during a later evolutionary period.", "distribution": [{"@type": "dcat:Distribution", "description": "Visit the original government dataset for complete information, documentation, and data access.", "downloadURL": "https://www.ncbi.nlm.nih.gov/pmc/articles/PMC33392/", "mediaType": "text/html", "title": "Official Government Data Source"}], "identifier": "https://healthdata.gov/api/views/j2u2-mbmj", "issued": "2025-07-14", "keyword": ["alternative-splicing", "gene-expression", "nervous-system", "nih", "rptrp-rho"], "landingPage": "https://healthdata.gov/d/j2u2-mbmj", "modified": "2025-09-06", "programCode": ["009:033"], "publisher": {"@type": "org:Organization", "name": "National Institutes of Health"}, "theme": ["NIH"], "title": "Genomic organization and alternative splicing of the human and mouse RPTP\u03c1 genes"}