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Table 2 The highly recurrent CNVs in schizophrenic subjects

From: Genetic copy number variants in sib pairs both affected with schizophrenia

Cytoband Gene symbol Aberration scoresa
   A2 B1 C2 D1 D2 E2 H1 I1
7q36.1 PRKAG2    -3.34 -3.25   -3.72   -2.94
8q11.21 CEBPD   -2.75   -3.68   -3.59   -3.03
9q31.2 KLF4   -2.58 -2.53 -3.55   -3.42   
9q34.2 RXRA    -3.12 -1.71   -1.67 -3.26 -2.53
  UBADC1   -1.73   -3.54     -3.05
  LCN6 -2.21 -1.97   -2.14   -3.27   -2.19
9q34.3 LCN8 -2.21 -1.97   -2.14   -3.27   -2.19
  C9orf37    -1.22   -3.07 3.09   
10q22.1 COL13A1   -1.52 -3.65 -3.3     
12q24.13 LHX5 -4.11 -3.79     -3.23   
15q26.1 RHCG -4.02 -4.26     -3.45   
17q25.2 SEPT9    -3.31 -3.34   -3.24   
19p13.3 STK11    -3.07     -2.68 -2.43
19q13.31 PVR    -3.09 -2.44 3.24    
21q21.1 BU678720   -2.79   -4.03 -3.81    
21q22.3 C21orf57    -3.85 -3.22     -2.94
  1. a The aberration scores (n) are calculated by using the Agilent aberration detection method: no change is defined as n = 0, loss as n < -1, and gain as n > 1. Bold type indicates CNS-related genes. Description and GenBank accession no.: Protein kinase, AMP-activated, gamma 2 non-catalytic subunit (PRKAG2 , NM_001040633), Kruppel-like factor 5 (KLF4, NM_001730); UBA domain containing 1 (UBADC1, NM_016172); lipocalin 6 (LCN6, NM_198946); lipocalin 8 (LCN8, NM_178469); chromosome 9 open reading frame 37 (C9orf37, NM_032937); collagen, type XIII, alpha 1(COL13A1, NM_001130103); Rh family, C glycoprotein (RHCG, NM_016321); septin 9 (SEPT9, NM_001113496); poliovirus receptor (PVR, NM_006505); and chromosome 21 open reading frame 57 (C21orf57, NM_058181).