Citations for
1DEL17Q21, KANSL1
Mutations in the chromatin modifier gene KANSL1 cause the 17q21.31 microdeletion syndrome.
Koolen DA, Kramer JM, Neveling K, Nillesen WM, Moore-Barton HL, Elmslie FV, Toutain A, Amiel J, Malan V, Tsai AC, Cheung SW, Gilissen C, Verwiel ET, Martens S, Feuth T, Bongers EM, de Vries P, Scheffer H, Vissers LE, de Brouwer AP, Brunner HG, Veltman JA, Schenck A, Yntema HG, de Vries BB.
Nat Genet at Genet. 2012 Apr 29. doi: 10.1038/ng.2262. [Epub ahead of print] 2012
2DEL17Q21, KANSL1
Mutations in KANSL1 cause the 17q21.31 microdeletion syndrome phenotype.
Zollino M, Orteschi D, Murdolo M, Lattante S, Battaglia D, Stefanini C, Mercuri E, Chiurazzi P, Neri G, Marangi G.
Nat Genet 44(6):636-8. doi: 10.1038/ng.2257. 2012
3ABHD12, ABHD12B, ABTB2, AGBL3, AMMECR1L, ANAPC15, ANKMY1, ANKRD16, ANKRD22, ANKRD29, ANKRD36, ANKRD40, ANKRD43, ANKRD44, APOPT1, ARHGAP30, ARL16, ARL17, ARL17P1, ARMC1, ATAD1, BRD9, C10orf126, C10orf132, C10orf57, C10orf58, C10orf84, C10orf85, C10orf88, C10orf90, C10orf91, C10orf92, C10orf93, C10orf95, C11orf10, C11orf36, C11orf41, C11orf42, C11orf45, C11orf46, C11orf52, C11orf53, C11orf57, C11orf58, C11orf61, C11orf63, C11orf64, C11orf66, C11orf71, C11orf72, C11orf76, C12orf23, C12orf26, C12orf28, C12orf32, C12orf33, C12orf34, C12orf36, C12orf45, C12orf48, C12orf54, C12orf60, C13orf16, C13orf26, C13orf27, C13orf28, C13orf29, C13orf30, C13orf33, C14orf109, C14orf126, C14orf128, C14orf138, C14orf148, C14orf152, C14orf177, C14orf178, C15orf26, C15orf32, C15orf33, C15orf34, C15orf40, C16orf58, C16orf61, C16orf74, C16orf78, C17orf44, C17orf50, C17orf54, C17orf57, C17orf58, C18orf16, C18orf18, C18orf22, C19orf18, C19orf22, C19orf23, C19orf28, C19orf30, C19orf36, C19orf48, C1orf106, C1orf109, C1orf57, C20orf103, C20orf106, C20orf108, C20orf112, C20orf144, C20orf149, C20orf165, C20orf166, C20orf194, C20orf197, C20orf39, C20orf62, C20orf79, C21orf128, C22orf13, C22orf27, C22orf36, C2orf24, C2orf48, C3orf14, C3orf17, C3orf18, C3orf22, C3orf24, C3orf25, C3orf26, C3orf31, C3orf32, C3orf33, C3orf36, C3orf37, C3orf38, C3orf45, C3orf46, C3orf54, C3orf62, C4orf36, C5orf23, C7orf38, C7orf45, C8orf44, C8orf45, C8orf46, C8orf74, C9orf116, C9orf70, CC2D2B, CCDC101, CCDC102A, CCDC103, CCDC117, CCDC124, CCDC37, CCDC38, CCDC46, CCDC48, CCDC58, CCDC58P1, CCDC68, CCDC70, CCDC74B, CCDC8, CCDC84, CCDC99, CFAP300, CFAP58, CFAP58, CHCHD5, CLDND2, COQ8B, COX14, CXorf21, CXorf38, CXorf42, DDRGK1, DEXI, DIPK2A, DNAJB8, DNAJC18, DNAJC5G, DPY19L1, DPY19L3, DPY19L4, DUS1L, DUS3L, EFCAB1, EFCAB2, EFCAB3, EFCAB4B, EFHA2, EFHB, ELP6, EMC3, EMC7, EPHX4, EXO5, FAM100B, FAM106A, FAM162B, FAM168A, FAM81A, FAM81B, FOPNL, HEATR3, HEATR4, HSFX2, IFT43, IL34, KANSL1, KLHL29, KLHL30, KLHL30, KLHL36, KNSTRN, LAMTOR1, LRRC20, LRRC24, LRRC34, MALSU1, MARCH9, MCU, MT1P3, NACC2, NCRNA00175, NJMUR1, NJMUR1, NKAPL, ODF3L2, OTUD7A, PID1, POMGNT2, PRIMPOL, PRR11, PRR12, RWDD2A, SS4RP1, TANGO2, TERB2, THOC6, TIMM29, TMEM101, TMEM106A, TMEM106C, TMEM107, TMEM108, TMEM109, TMEM110, TMEM116, TMEM217, TMEM229B, TMEM260, TRIM65, TTC17, TTC6, TTPAL, TUBB6, WDR72, WDR85, ZBTB45, ZBTB5, ZBTB9, ZNF385B, ZNF439, ZNF440, ZNF454, ZNF485, ZNF486, ZNF497, ZNF509, ZNF519, ZNF524, ZNF613, ZNF625, ZNF643, ZNRF3, ZSCAN1, ZSCAN23, ZSCAN5A, ZSWIM1, ZSWIM3
The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC).
Gerhard DS, Wagner L, Feingold EA, Shenmen CM, Grouse LH, Schuler G, Klein SL, Old S, Rasooly R, Good P, Guyer M, Peck AM, Derge JG, Lipman D, Collins FS, Jang W, Sherry S, Feolo M, Misquitta L, Lee E, Rotmistrovsky K, Greenhut SF, Schaefer CF, Buetow K, Bonner TI, Haussler D, Kent J, Kiekhaus M, Furey T, Brent M, Prange C, Schreiber K, Shapiro N, Bhat NK, Hopkins RF, Hsie F, Driscoll T, Soares MB, Casavant TL, Scheetz TE, Brown-stein MJ, Usdin TB, Toshiyuki S, Carninci P, Piao Y, Dudekula DB, Ko MS, Kawakami K, Suzuki Y, Sugano S, Gruber CE, Smith MR, Simmons B, Moore T, Waterman R, Johnson SL, Ruan Y, Wei CL, Mathavan S, Gunaratne PH, Wu J, Garcia AM, Hulyk SW, Fuh E, Yuan Y, Sneed A, Kowis C, Hodgson A, Muzny DM, McPherson J, Gibbs RA, Fahey J, Helton E, Ketteman M, Madan A, Rodrigues S, Sanchez A, Whiting M, Madari A, Young AC, Wetherby KD, Granite SJ, Kwong PN, Brinkley CP, Pearson RL, Bouffard GG, Blakesly RW, Green ED, Dickson MC, Rodriguez AC, Grimwood J, Schmutz J, Myers RM, Butterfield YS, Griffith M, Griffith OL, Krzywinski MI, Liao N, Morin R, Palmquist D, Petrescu AS, Skalska U, Smailus DE, Stott JM, Schnerch A, Schein JE, Jones SJ, Holt RA, Baross A, Marra MA, Clifton S, Makowski KA, Bosak S, Malek J; MGC Project Team.
Genome Res 14(10B):2121-7. Erratum in: Genome Res. 2006 Jun;16(6):804. Morrin, Ryan [corrected to Morin, Ryan]. 2004
4AGBL5, DEPTOR, KANSL1, KLHL7, LIMCH1, OLA1, TMEM126A, TMEM50B
Systematic subcellular localization of novel proteins identified by large-scale cDNA sequencing.
Simpson JC, Wellenreuther R, Poustka A, Pepperkok R, Wiemann S.
EMBO Rep 1(3):287-92. 2000