PHF6

PHD finger protein 6 is a protein that in humans is encoded by the PHF6 gene.

PHF6
Available structures PDB Ortholog search: PDBe RCSB List of PDB id codes 4NN2, 4R7A
Identifiers
Aliases	PHF6, BFLS, BORJ, CENP-31, PHD finger protein 6
External IDs	OMIM: 300414; MGI: 1918248; HomoloGene: 12375; GeneCards: PHF6; OMA:PHF6 - orthologs
Gene location (Human) Chr. X chromosome (human) Band Xq26.2 Start 134,373,288 bp End 134,428,791 bp
Gene location (Mouse) Chr. X chromosome (mouse) Band X|X A5 Start 52,001,143 bp End 52,045,820 bp
RNA expression pattern Bgee Human Mouse (ortholog) Top expressed in corpus epididymis oocyte endothelial cell germinal epithelium secondary oocyte ganglionic eminence pancreatic epithelial cell palpebral conjunctiva epithelium of nasopharynx Brodmann area 23 Top expressed in hand superior cervical ganglion ventricular zone genital tubercle tail of embryo medial ganglionic eminence zygote epiblast maxillary prominence trigeminal ganglion More reference expression data BioGPS More reference expression data
Gene ontology Molecular function tubulin binding enzyme binding scaffold protein binding DNA binding ribonucleoprotein complex binding histone binding phosphoprotein binding histone deacetylase binding protein binding metal ion binding RNA binding DNA-binding transcription repressor activity, RNA polymerase II-specific sequence-specific DNA binding Cellular component nucleolus chromosome, centromeric region nucleus kinetochore nucleoplasm chromosome Biological process regulation of transcription, DNA-templated transcription, DNA-templated negative regulation of transcription by RNA polymerase II blastocyst hatching Sources:Amigo / QuickGO
Orthologs Species Human Mouse Entrez 84295 70998 Ensembl ENSG00000156531 ENSMUSG00000025626 UniProt Q8IWS0 Q9D4J7 RefSeq (mRNA) NM_032458 NM_001015877 NM_032335 NM_001290546 NM_027642 RefSeq (protein) NP_001015877 NP_115711 NP_115834 NP_001277475 NP_081918 Location (UCSC) Chr X: 134.37 – 134.43 Mb Chr X: 52 – 52.05 Mb PubMed search
Wikidata
View/Edit Human View/Edit Mouse

This gene is a member of the plant homeodomain (PHD)-like finger (PHF) family. It encodes a protein with two atypical PHD-type zinc finger domains, indicating a potential role in transcriptional regulation, that localizes to the nucleolus.

Mutations

Mutations affecting the coding region of this gene or the splicing of the transcript have been associated with Börjeson-Forssman-Lehmann syndrome (BFLS), a disorder characterized by mental retardation, epilepsy, hypogonadism, hypometabolism, obesity, swelling of subcutaneous tissue of the face, narrow palpebral fissures, and large ears. Alternate transcriptional splice variants, encoding different isoforms, have been characterized.

The PHF6 gene in humans is also frequently mutated in human hematological malignancies, including T-cell acute lymphoblastic Leukemia (T-ALL) and Acute Myeloid Leukemia (AML) and at least two BFLS patients have developed leukemia or lymphoma. PHF6 has been shown to be important for the regulation of blood stem and progenitor cells and loss of PHF6 protein synergizes with over-expression of the TLX3 protein to cause lymphoid neoplasms.

Further reading

• Nagase T, Nakayama M, Nakajima D, Kikuno R, Ohara O (April 2001). "Prediction of the coding sequences of unidentified human genes. XX. The complete sequences of 100 new cDNA clones from brain which code for large proteins in vitro". DNA Research. 8 (2): 85–95. doi:10.1093/dnares/8.2.85. PMID 11347906.
• Baumstark A, Lower KM, Sinkus A, Andriuskeviciute I, Jurkeniene L, Gécz J, Just W (April 2003). "Novel PHF6 mutation p.D333del causes Börjeson-Forssman-Lehmann syndrome". Journal of Medical Genetics. 40 (4): 50e–50. doi:10.1136/jmg.40.4.e50. PMC 1735415. PMID 12676923.
• Dattani MT (December 2003). "Borjeson-Forssman-Lehmann syndrome: a novel pituitary phenotype due to mutation in a novel gene". Journal of Pediatric Endocrinology & Metabolism. 16 (9): 1207–9. doi:10.1515/jpem.2003.16.9.1207. PMID 14714741. S2CID 45542882.
• Birrell G, Lampe A, Richmond S, Bruce SN, Gécz J, Lower K, et al. (December 2003). "Borjeson-Forssman-Lehmann syndrome and multiple pituitary hormone deficiency". Journal of Pediatric Endocrinology & Metabolism. 16 (9): 1295–300. doi:10.1515/jpem.2003.16.9.1295. PMID 14714754. S2CID 10327867.
• Turner G, Lower KM, White SM, Delatycki M, Lampe AK, Wright M, et al. (March 2004). "The clinical picture of the Börjeson-Forssman-Lehmann syndrome in males and heterozygous females with PHF6 mutations". Clinical Genetics. 65 (3): 226–32. doi:10.1111/j.0009-9163.2004.00215.x. PMID 14756673. S2CID 24602739.
• Lower KM, Solders G, Bondeson ML, Nelson J, Brun A, Crawford J, et al. (October 2004). "1024C> T (R342X) is a recurrent PHF6 mutation also found in the original Börjeson-Forssman-Lehmann syndrome family". European Journal of Human Genetics. 12 (10): 787–9. doi:10.1038/sj.ejhg.5201228. PMID 15241480. S2CID 7327686.
• Vallée D, Chevrier E, Graham GE, Lazzaro MA, Lavigne PA, Hunter AG, Picketts DJ (October 2004). "A novel PHF6 mutation results in enhanced exon skipping and mild Börjeson-Forssman-Lehmann syndrome". Journal of Medical Genetics. 41 (10): 778–83. doi:10.1136/jmg.2004.020370. PMC 1735599. PMID 15466013.
• Andersen JS, Lam YW, Leung AK, Ong SE, Lyon CE, Lamond AI, Mann M (January 2005). "Nucleolar proteome dynamics". Nature. 433 (7021): 77–83. Bibcode:2005Natur.433...77A. doi:10.1038/nature03207. PMID 15635413. S2CID 4344740.
• Crawford J, Lower KM, Hennekam RC, Van Esch H, Mégarbané A, Lynch SA, et al. (March 2006). "Mutation screening in Borjeson-Forssman-Lehmann syndrome: identification of a novel de novo PHF6 mutation in a female patient". Journal of Medical Genetics. 43 (3): 238–43. doi:10.1136/jmg.2005.033084. PMC 2563250. PMID 15994862.
• Olsen JV, Blagoev B, Gnad F, Macek B, Kumar C, Mortensen P, Mann M (November 2006). "Global, in vivo, and site-specific phosphorylation dynamics in signaling networks". Cell. 127 (3): 635–48. doi:10.1016/j.cell.2006.09.026. PMID 17081983. S2CID 7827573.

External links

• PHF6+protein,+human at the U.S. National Library of Medicine Medical Subject Headings (MeSH)

This article incorporates text from the United States National Library of Medicine, which is in the public domain.