A2BP1, ataxin 2-binding protein 1 (605104); 16p13 |
ABAT, 4-(gamma)-aminobutyrate transferase (137150); 16p13.3 |
ACTB, actin-beta (102630), 7p22.1 |
ADSL, adenylosuccinate lyase (608222); 22q13.1 |
AKAP8, A-kinase anchor protein 6 (604692) 19p13.12 |
AMPA 1, GRIA1 glutamate receptor, ionotropic (138248); 5q33 |
ANKRD11, ankyrin repeat domain-containing protein 11 (611192); 16q24.3 |
APBA2, amyloid beta A4 precursor protein-binding, family A (602712); 15q13.1 |
APC, adenomatous polyposis coli (611731); 5q21q22 |
AQP4, aquaporin 4; (600308) 18q11.2q12.1 |
ARX, aristaless-related homeobox, X-linked (300382); Xp22.13 |
AVPR1A, arginine vasopressin receptor 1A (600821); 12q14q15 |
BDNF, brain-derived neurotropic factor (115505); 11p13 |
CACNA1C, calcium channel, voltage-dependent, L type, alpha-1C subunit (114205); 12p13.3 |
CADPS2, calcium-dependent activator protein for secretion 2 (609978); 7q31.3 |
CDH9, cadherin 9 (609974); 5p14 CDH10, cadherin 10 (604555); |
CDH10, cadherin 10 (604555); 5p14p13 |
CENTG2, centaurin, gamma-2 (608651); 2q37.3 |
CHAT, choline acetyltransferase (118490); 10q11.23 |
CHRNA7, cholinergic receptor neuronal nicotinic alpha polypeptide 7 (118511); 15q14 |
CNTN3, contactin 3 (601325); 3p26 |
CNTN4, contactin 4 (607280); 3 p26p25 |
CNTNAP2, contactin-associated protein-like 2 (604569); 7q35q36 |
COMT, catechol-o-methyltransferase (116790); 22q11.2 |
CSMD3, cub and sushi multiple domains 3 (608399); 8q23.3 |
CYFIP1, cytoplastmic FMRP-interacting protein 1 (606322); 15q11 |
DIA1, CXORF36, deleted in autism 1; chromosome 3 open reading frame (612200); Xp11.3 |
DISC1, disrupted in schizophrenia 1 (605210); 1q42.2 |
DLG1, discs large, drosophila, homolog of (601104); 3q29 |
DLX1, distal-less homeobox 1 (600029); 2q32 |
DLX2, distal-less homeobox 2 (126255); 2q32 |
EIF4E, eucaryotic translation initiation factor 4E (133440); 4q21q25 |
EN2, engrailed 2 (131310); 7q36 |
EPC2, enhancer of polycomb, Drosophila, homolog of, 2 (611000); 2q23.1 |
FABP5; FABP7, fatty acid binding protein 5 (605168); 8q21.13; and 7 (602965); 6q22.31 |
FHIT, fragile histidine triad gene, fragile site (601153); 3p14.2 |