Table 4.
Integrating Small De Novo Deletions in TADA Identified 65 ASD Genes
dnLoF Count | FDR ≤ 0.01 | 0.01 < FDR ≤ 0.05 | 0.05 < FDR ≤ 0.1 |
---|---|---|---|
≥2 | ADNP, ANK2, ARID1B, ASH1L, CHD2, CHD8, CUL3, DSCAM, DYRK1A, GRIN2B, KATNAL2, KDM5B, KMT2C, NCKAP1, POGZ, SCN2A, SUV420H1, SYNGAP1, TBR1, TCF7L2, TNRC6B, WAC | BCL11A, FOXP1, GIGYF1, ILF2, KDM6B, PHF2, RANBP17, SPAST, WDFY3 | DIP2A, KMT2E |
1 | NRXN1, PTEN, SETD5, SHANK2, SHANK3, TRIP12 | DNMT3A, GABRB3, KAT2B, MFRP, MYT1L, P2RX5 | AKAP9, APH1A, CTTNBP2, ERBB2IP, ETFB, INTS6, IRF2BPL, MBD5, NAA15, NINL, OR52M1, PTK7, TRIO, USP45 |
0 | – | MIB1, SLC6A1, ZNF559 | ACHE, CAPN12, NLGN3 |
Genes with a small de novo deletion are in bold. FDR, false discovery rate.