WHSC1L1

Wolf-Hirschhorn syndrome candidate 1-like 1, also known as WHSC1L1, is a human gene.cite web | title = Entrez Gene: WHSC1L1 Wolf-Hirschhorn syndrome candidate 1-like 1| url = http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=54904| accessdate = ]

PBB_Summary
section_title =
summary_text = This gene is related to the Wolf-Hirschhorn syndrome candidate-1 gene and encodes a protein with PWWP (proline-tryptophan-tryptophan-proline) domains. The function of the protein has not been determined. Two alternatively spliced variants have been described.cite web | title = Entrez Gene: WHSC1L1 Wolf-Hirschhorn syndrome candidate 1-like 1| url = http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=54904| accessdate = ]

References

Further reading

PBB_Further_reading
citations =
*cite journal | author=Stec I, Nagl SB, van Ommen GJ, den Dunnen JT |title=The PWWP domain: a potential protein-protein interaction domain in nuclear proteins influencing differentiation? |journal=FEBS Lett. |volume=473 |issue= 1 |pages= 1–5 |year= 2000 |pmid= 10802047 |doi=
*cite journal | author=Angrand PO, Apiou F, Stewart AF, "et al." |title=NSD3, a new SET domain-containing gene, maps to 8p12 and is amplified in human breast cancer cell lines. |journal=Genomics |volume=74 |issue= 1 |pages= 79–88 |year= 2001 |pmid= 11374904 |doi= 10.1006/geno.2001.6524
*cite journal | author=Stec I, van Ommen GJ, den Dunnen JT |title=WHSC1L1, on human chromosome 8p11.2, closely resembles WHSC1 and maps to a duplicated region shared with 4p16.3. |journal=Genomics |volume=76 |issue= 1-3 |pages= 5–8 |year= 2001 |pmid= 11549311 |doi= 10.1006/geno.2001.6581
*cite journal | author=Rosati R, La Starza R, Veronese A, "et al." |title=NUP98 is fused to the NSD3 gene in acute myeloid leukemia associated with t(8;11)(p11.2;p15). |journal=Blood |volume=99 |issue= 10 |pages= 3857–60 |year= 2002 |pmid= 11986249 |doi=
*cite journal | author=Strausberg RL, Feingold EA, Grouse LH, "et al." |title=Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences. |journal=Proc. Natl. Acad. Sci. U.S.A. |volume=99 |issue= 26 |pages= 16899–903 |year= 2003 |pmid= 12477932 |doi= 10.1073/pnas.242603899
*cite journal | author=Ota T, Suzuki Y, Nishikawa T, "et al." |title=Complete sequencing and characterization of 21,243 full-length human cDNAs. |journal=Nat. Genet. |volume=36 |issue= 1 |pages= 40–5 |year= 2004 |pmid= 14702039 |doi= 10.1038/ng1285
*cite journal | author=Gerhard DS, Wagner L, Feingold EA, "et al." |title=The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC). |journal=Genome Res. |volume=14 |issue= 10B |pages= 2121–7 |year= 2004 |pmid= 15489334 |doi= 10.1101/gr.2596504
*cite journal | author=Tonon G, Wong KK, Maulik G, "et al." |title=High-resolution genomic profiles of human lung cancer. |journal=Proc. Natl. Acad. Sci. U.S.A. |volume=102 |issue= 27 |pages= 9625–30 |year= 2005 |pmid= 15983384 |doi= 10.1073/pnas.0504126102
*cite journal | author=Kim SM, Kee HJ, Eom GH, "et al." |title=Characterization of a novel WHSC1-associated SET domain protein with H3K4 and H3K27 methyltransferase activity. |journal=Biochem. Biophys. Res. Commun. |volume=345 |issue= 1 |pages= 318–23 |year= 2006 |pmid= 16682010 |doi= 10.1016/j.bbrc.2006.04.095

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