Citations for
1NAALADL2
Genetic alterations in the 3q26.31-32 locus confer an aggressive prostate cancer phenotype.
Simpson BS, Camacho N, Luxton HJ, Pye H, Finn R, Heavey S, Pitt J, Moore CM, Whitaker HC.
Commun Biol. Aug 14;3(1):440. doi: 10.1038/s42003-020-01175-x. 2020
2NAALADL2, YIPF7
Identification of genetic susceptibility loci for intestinal Behçet's disease.
Kim SW, Jung YS, Ahn JB, Shin ES, Jang HW, Lee HJ, Il Kim T, Kim DY, Bang D, Kim WH, Cheon JH.
Sci Rep. Jan 3;7:39850. doi: 10.1038/srep39850 2017
3NAALADL2
N-acetyl-L-aspartyl-L-glutamate peptidase-like 2 is overexpressed in cancer and promotes a pro-migratory and pro-metastatic phenotype.
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.
Oncogene Nov 6;33(45):5274-87. doi: 10.1038/onc.2013.464. Epub 2013 Nov 18. 2014
4DEL3QO, NAALADL2
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.
Millson A, Lagrave D, Willis MJ, Rowe LR, Lyon E, South ST.
Am J Med Genet A. Jan;158A(1):159-65. doi: 10.1002/ajmg.a.34349. Epub 2011 Nov 21. 2012
5NAALADL2, ZFHX3
A genome-wide association study identifies novel and functionally related susceptibility Loci for Kawasaki disease.
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.
PLoS Genet 5(1):e1000319. Epub 2009 Jan 9. 2009
6CDLS, DUP3QD, NAALADL2
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.
Borg K, Stankiewicz P, Bocian E, Kruczek A, Obersztyn E, Lupski JR, Mazurczak T.
Hum Genet 118(2):267-75. Epub 2005 Nov 15. Erratum in: Hum Genet. 2006 Jan;118(5):668. 2005
7CDLS,DUP3QD,NAALADL2
A giant novel gene undergoing extensive alternative splicing is severed by a Cornelia de Lange-associated translocation breakpoint at 3q26.3.
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.
Hum Genet 115(2):139-48. Epub 2004 May 27. 2004