Biology:OFD1

Short description: Mammalian protein found in Homo sapiens

Generic protein structure example

Oral-facial-digital syndrome 1 protein is a protein that in humans is encoded by the OFD1 gene.

Human chromosomal region Xp22.3-p21.3 comprises the area between the pseudoautosomal boundary and the Duchenne muscular dystrophy gene (MIM 300377). This region harbors several disease loci, including OFD1 (MIM 311200), CFNS (MIM 304110), DFN6 (MIM 300066), and SEDT (MIM 313400). It also contains a region of homology with both the short and the long arms of the Y chromosome and undergoes frequent chromosomal rearrangements.[supplied by OMIM]

See also

• Orofaciodigital syndrome 1
• Simpson–Golabi–Behmel syndrome

External links

• GeneReviews/NCBI/NIH/UW entry on Oral-Facial-Digital Syndrome Type I

Further reading

• "A 6-Mb YAC contig in Xp22.1-p22.2 spanning the DXS69E, XE59, GLRA2, PIGA, GRPR, CALB3, and PHKA2 genes". Genomics 25 (3): 691–700. 1995. doi:10.1016/0888-7543(95)80012-B. PMID 7759104. 
• "Oligo-capping: a simple method to replace the cap structure of eukaryotic mRNAs with oligoribonucleotides". Gene 138 (1–2): 171–4. 1994. doi:10.1016/0378-1119(94)90802-8. PMID 8125298. 
• "Construction and characterization of a full length-enriched and a 5'-end-enriched cDNA library". Gene 200 (1–2): 149–56. 1997. doi:10.1016/S0378-1119(97)00411-3. PMID 9373149. 
• "Mapping of a new SGBS locus to chromosome Xp22 in a family with a severe form of Simpson-Golabi-Behmel syndrome". Am. J. Hum. Genet. 65 (3): 779–83. 1999. doi:10.1086/302527. PMID 10441586. 
• "Identification of the gene for oral-facial-digital type I syndrome". Am. J. Hum. Genet. 68 (3): 569–76. 2001. doi:10.1086/318802. PMID 11179005. 
• "A new sequence motif linking lissencephaly, Treacher Collins and oral-facial-digital type 1 syndromes, microtubule dynamics and cell migration". Hum. Mol. Genet. 10 (24): 2813–20. 2002. doi:10.1093/hmg/10.24.2813. PMID 11734546. 
• "Four novel mutations in the OFD1 (Cxorf5) gene in Finnish patients with oral-facial-digital syndrome 1". J. Med. Genet. 39 (4): 292–6. 2002. doi:10.1136/jmg.39.4.292. PMID 11950863. 
• "Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences". Proc. Natl. Acad. Sci. U.S.A. 99 (26): 16899–903. 2003. doi:10.1073/pnas.242603899. PMID 12477932. Bibcode: 2002PNAS...9916899M. 
• "OFD1, the gene mutated in oral-facial-digital syndrome type 1, is expressed in the metanephros and in human embryonic renal mesenchymal cells". J. Am. Soc. Nephrol. 14 (3): 680–9. 2003. doi:10.1097/01.ASN.0000054497.48394.D2. PMID 12595504. 
• "Characterization of the OFD1/Ofd1 genes on the human and mouse sex chromosomes and exclusion of Ofd1 for the Xpl mouse mutant". Genomics 81 (6): 560–9. 2004. doi:10.1016/S0888-7543(03)00091-0. PMID 12782125. 
• "Proteomic characterization of the human centrosome by protein correlation profiling". Nature 426 (6966): 570–4. 2003. doi:10.1038/nature02166. PMID 14654843. Bibcode: 2003Natur.426..570A. 
• "OFD1 is a centrosomal/basal body protein expressed during mesenchymal-epithelial transition in human nephrogenesis". J. Am. Soc. Nephrol. 15 (10): 2556–68. 2005. doi:10.1097/01.ASN.0000140220.46477.5C. PMID 15466260. 
• "The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC)". Genome Res. 14 (10B): 2121–7. 2004. doi:10.1101/gr.2596504. PMID 15489334. 
• "Clinical, molecular, and genotype-phenotype correlation studies from 25 cases of oral-facial-digital syndrome type 1: a French and Belgian collaborative study". J. Med. Genet. 43 (1): 54–61. 2006. doi:10.1136/jmg.2004.027672. PMID 16397067. 
• "A novel X-linked recessive mental retardation syndrome comprising macrocephaly and ciliary dysfunction is allelic to oral-facial-digital type I syndrome". Hum. Genet. 120 (2): 171–8. 2007. doi:10.1007/s00439-006-0210-5. PMID 16783569.