Skip to main content
. Author manuscript; available in PMC: 2021 Apr 19.
Published in final edited form as: Schizophr Res. 2020 Jan 9;216:450–459. doi: 10.1016/j.schres.2019.10.039

Table 4.

Regions of homozygosity having shared haplotypes that are over-represented in schizophrenia cases.

Major Haplotype Gene
Chromosome Position Band Size (kilobases) SNP count Case : Control N Case : Control Symbol Name
1 89,116,300–89,286,673 1p22.2 170.4 11 9:0 3 7:0 PRKN2a Protein kinase N2
1 89,530,860–89,721,862 1p22.2 191 14 9:0 5 5:0 GBP1b; GBP2; GBP4; GBP7 Guanylate binding proteins
14 30,070,659–30,290,431 14q12 219.8 19 9:0 3 7:0 PRKD1c Protein kinase D1
14 30,991,559–31,172,582 14q12 181 14 9:0 4 6:0 G2E3 SCFD1d G2/M Phase-specific E3 Ubiquitin Ligase SEC1 Family Domain Containing 1
1 146,660,395–146,736,137 1q21.1 75.7 11 7:0 4 4:0 FMO5e CHD1Lf Flavin Containing Monooxygenase 5 Chromodomain Helicase DNA-binding Protein 1 Like
12 8,698,471–8,820,124 12p13.31 121.7 13 6:0 4 3:0 AICDA MFAP5 Activation-induced Cytidine Deaminase Microfibrillar-associated Protein 5
a

ROH in PRKN2 (NM_006256) contained 16 of 22 exons.

b

ROH in GPB1 (NM_002053) contained one of 11 exons.

c

ROH in PRKD1 (NM_002742) contained 13 of 18 exons.

d

ROH in SCFD1 (NM_016106) contained 16 of 25 exons.

e

ROH in FMO5 (NM_001461) contained 8 of 9 exons.

f

ROH in CHD1L (NM_004284) contained 7 of 23 exons.