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Search diseases:
OMIM ID
181500
OMIM term:
SCHIZOPHRENIA; SCZD
Alternative terms:
(∗) Location:
10q22.3 11p14.1 11q14-q21 12q24.11 13q14.2 13q32 13q33.2 14q32.33 18p 1p36.2 1p36.22 1q32.1 1q42.2 22q11.21 22q12.3 3p25.2 3q13.31 5q23-q35 6p22.3 6p23 6q13-q26 8p21
(†) Associated OMIM genes:
CHI3L1
COMT CATECHOL-O-METHYLTRANSFERASE ACTIVITY, LOW, IN RED CELLS, INCLUDED
DISC1
DRD3
GPR48
HTR2A
MTHFR
RTN4R
SYN2
(‡) Associated MGI genes:
Akt1
Avpr1a
Chst3
Cplx2
Ctsc
Disc1
Grin1
Lrrtm1
Mdk
Mtap6
Nr4a2
Nrg1
Nrxn1
Plcb1
Ppm1g
Slc6a3
Snap25
Srr
Taar1
Zic2
ckr
Mouse
Zebrafish
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