NIPA1, non-imprinted gene in Prader-Willi/Angelman syndrome chromosome region 1 (608145); 15q11.1

NLGN3, NLGN4, NLGN4Y neuroligin 3 (300336); Xq13.1, 4(300427);Xp22.33, Y-linked (400028); Yq11.2

NRXN1, neurexin-1 (600565); 1p16.3

NSD1, nuclear receptor-binding set domain protein 1 (606681); 5q35.3

OXTR, oxytocin receptor (167055); 3p26.2

PAK2, p21-activated kinase2 (605022); 3q29

PAX3, paired box gene 3 (606597); 2q35

PCDH10, protocadherin 10 (608286); 4q28.3

PDE4D, phosphodiesterase 4D (600129); 5q12

PHF8, PHD finger protein 8 (300560); Xp11.2

PITX1, paired-like homeodomain transcription factor 1 (602149); 5q31

PRKCB1, protein kinase C beta-1 (176970); 16p11.2

PTEN, phosphatase and tensin homolog (601728); 10q23.31

PTPN9, protein-tyrosine phosphatase nonreceptor-type 9 (600768); (15q22q23)

RAB11FIP5; RAB11 family-interacting protein 5 (605536); 1p13

RAI1, retinoic acid induced gene (607642); 17p11.2

RAPGEF4, RAP, guanine nucleotide exchange factor (606058); 2q31.1

RASA1, RAS p21 protein activator 1 (139150); 5q14.3

RBM8A, RNAN-binding motif protein 8A (605313); 1q21.1

REEP3, receptor expression-enhancing protein 3; 10q21.3

RELN, Reelin, from mouse mutation “reeler” with poor coordination (600514); 7q22.1

RNF8, Ring finger protein 8 (611685); 6p21.3

RPS6KA3, ribosomal protein X6 kinase, 90-Kd, 3 (3000075); Xp22.12 and 7Z

SCN1A, SCN7A, sodium channel neuronal type I alpha subunit (182389); 2q24 and VII (182292); 2q21q23

SCT, secretin (182099); 11p15.5

SEMA5A, semaphoring 5A (609297); 5p15.2

SHANK3, SH3 and multiple ankyrin repeat domains 3 (606230); 22q13.3

SLC1A3, solute carrier family 1 (glial high affinity glutamate transporter, member 3-600111); 5p13

SLC4A10, solute carrier family 4 (sodium bicarbonate transporter-like) member 10 (605556); 2q24.2

SLC6A3/DAT1, SLC6A4, solute carrier family 6, member 3-dopamine transporter (126455); 5p15.3 and 4 (182138); 17q11.1q12

SLC9A9/(NHE9 sodium/hydrogen exchanger 9/solute carrier family 9 (608396); 3q24

SLC18A3, solute carrier family 18 (vesicular acetylcholine), member 3 (600336); 10q11.23

SLC25A12, solute carrier family 25 (mitochondrial carrier, ARALAR member (603667); 2q24

SLC40A1, solute carrier family 40 (iron-regulated transporter), member 1 (604653); 2q32

SSBP1, single-stranded DNA-binding protein 1 (600439); 7q34

ST7, RAY1, suppressor of tumorigenicity (600833); 7q31.1

STK, serine/threonine protein kinase 39 (607648); 2q24.3