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Table 2 DCX, COMT and FMR1 gene correlates associated with intellectual disability

From: Connecting DCX, COMT and FMR1 in social behavior and cognitive impairment

DCX + 

ACTB, ACTG1, ADNP, ARID1A, ARID1B, AUTS2, BBS9, CASK, CHAMP1, CTCF, DCHS1, DYRK1A, EDC3, EFTUD2, EHMT1, EML1, EXT2, FAT4, FGD1, FOXG1, FRMD4A, FTSJ1, FXR2, GATAD2B, GNB1, IGBP1, KAT6A, KIAA2022, LMAN2L, MCPH1, NONO, OPHN1, POGZ, RBMX, RSPRY1, SETBP1, SMARCA4, SMARCB1, SMC3, SOX11, TAF2, TCF4, TTI2, TUBGCP4, ZC4H2, ZEB2, ZNF711

DCX −

BCAP31, MAP2K1

COMT + 

BCAP31, CHI3L2, CLIC2, HEPACAM, PGAP3, PIGV, PPIC, SLC6A8, TECR, VWA3B

COMT −

ATP8A2, ATRX, AUTS2, BRWD3, CHAMP1, CTCF, DDX3X, EML1, FAT4, FXR2, GATAD2B, KDM6A, KIAA2022, MCPH1, MED13L, NUFIP1, PAK3, PGAP1, SETBP1, SOX5, TAF2, TCF4, TTC21B, UPF3B

FMR1 + 

AMMECR1, ATRX, BRWD3, COG6, CRBN, CUL4B, FMR1, KIAA0196, KIAA1033, NIPBL, NUFIP1, NUFIP2, RAB3GAP2, RAD21, RBBP8, RPS6KA3, TBL1XR1, TDP2, TTC21B, USP9X, ZDHHC15

FMR1 −

No associated genes

  1. Positive and negative associations are indicated with “+” and “−” respectively