1 | NAALADL2
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| Genetic alterations in the 3q26.31-32 locus confer an aggressive prostate cancer phenotype.
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| Simpson BS, Camacho N, Luxton HJ, Pye H, Finn R, Heavey S, Pitt J, Moore CM, Whitaker HC.
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| Commun Biol. Aug 14;3(1):440. doi: 10.1038/s42003-020-01175-x. 2020
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2 | NAALADL2, YIPF7
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| Identification of genetic susceptibility loci for intestinal Behçet's disease.
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| Kim SW, Jung YS, Ahn JB, Shin ES, Jang HW, Lee HJ, Il Kim T, Kim DY, Bang D, Kim WH, Cheon JH.
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| Sci Rep. Jan 3;7:39850. doi: 10.1038/srep39850 2017
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3 | NAALADL2
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| N-acetyl-L-aspartyl-L-glutamate peptidase-like 2 is overexpressed in cancer and promotes a pro-migratory and pro-metastatic phenotype.
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| Whitaker HC, Shiong LL, Kay JD, Grönberg H, Warren AY, Seipel A, Wiklund F, Thomas B, Wiklund P, Miller JL, Menon S, Ramos-Montoya A, Vowler SL, Massie C, Egevad L, Neal DE.
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| Oncogene Nov 6;33(45):5274-87. doi: 10.1038/onc.2013.464. Epub 2013 Nov 18. 2014
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4 | DEL3QO, NAALADL2
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| Chromosomal loss of 3q26.3-3q26.32, involving a partial neuroligin 1 deletion, identified by genomic microarray in a child with microcephaly, seizure disorder, and severe intellectual disability.
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| Millson A, Lagrave D, Willis MJ, Rowe LR, Lyon E, South ST.
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| Am J Med Genet A. Jan;158A(1):159-65. doi: 10.1002/ajmg.a.34349. Epub 2011 Nov 21. 2012
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5 | NAALADL2, ZFHX3
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| A genome-wide association study identifies novel and functionally related susceptibility Loci for Kawasaki disease.
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| Burgner D, Davila S, Breunis WB, Ng SB, Li Y, Bonnard C, Ling L, Wright VJ, Thalamuthu A, Odam M, Shimizu C, Burns JC, Levin M, Kuijpers TW, Hibberd ML; International Kawasaki Disease Genetics Consortium.
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| PLoS Genet 5(1):e1000319. Epub 2009 Jan 9.
2009
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6 | CDLS, DUP3QD, NAALADL2
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| Molecular analysis of a constitutional complex genome rearrangement with 11 breakpoints involving chromosomes 3, 11, 12, and 21 and a approximately 0.5-Mb submicroscopic deletion in a patient with mild mental retardation.
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| Borg K, Stankiewicz P, Bocian E, Kruczek A, Obersztyn E, Lupski JR, Mazurczak T.
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| Hum Genet 118(2):267-75. Epub 2005 Nov 15. Erratum in: Hum Genet. 2006 Jan;118(5):668.
2005
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7 | CDLS,DUP3QD,NAALADL2
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| A giant novel gene undergoing extensive alternative splicing is severed by a Cornelia de Lange-associated translocation breakpoint at 3q26.3.
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| Tonkin ET, Smith M, Eichhorn P, Jones S, Imamwerdi B, Lindsay S, Jackson M, Wang TJ, Ireland M, Burn J, Krantz ID, Carr P, Strachan T.
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| Hum Genet 115(2):139-48. Epub 2004 May 27. 2004
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