Table 1.
AutDB Description | Ptenm3m4 Expression | |||
---|---|---|---|---|
| ||||
Gene | Alteration in ASD | Variant categories observed | Log2(FC) | q-value |
CELF6 | Genetic association/Rare single gene variant/Functional | Deletions | −0.465 | 0.025 |
GALNT13 | Rare single gene variant | −0.429 | 0.004 | |
| ||||
ARHGAP15 | Rare single gene variant | Deletions, other | −0.529 | 0.003 |
CHRNB3 | Rare single gene variant | −0.962 | 0.046 | |
NELL1 | Genetic association | −0.386 | 0.008 | |
PCDH15 | Genetic association | 0.637 | 0.001 | |
| ||||
ADCY5 | Rare single gene variant | Deletions, missense mutations | −0.365 | 0.016 |
AGMO | Genetic association | 0.501 | 0.042 | |
DOCK10 | Rare single gene variant | 0.529 | 0.001 | |
PTCHD1 | Rare single gene variant | −0.350 | 0.049 | |
SYN2 | Genetic association | 0.401 | 0.016 | |
| ||||
CADPS2 | Rare single gene variant | Deletions, missense mutations, other | −0.325 | 0.049 |
GPR37 | Rare single gene variant | 0.524 | 0.001 | |
GRIK2 | Genetic Association | −0.531 | 0.001 | |
IL1RAPL1 | Rare single gene variant | −0.402 | 0.012 | |
KANK1 | Rare single gene variant | 0.586 | 0.001 | |
| ||||
AHI1 | Rare single gene variant | Deletions, duplications, missense mutations, other | −0.648 | 0.001 |
CHD2 | Multigenic CNV | −0.374 | 0.039 | |
CNTN5 | Rare single gene variant | −0.533 | 0.001 | |
CNTNAP2 | Syndromic | −0.341 | 0.037 | |
CREBBP | Syndromic | −0.324 | 0.050 | |
CTTNBP2 | Rare single gene variant | −0.405 | 0.005 | |
DCX | Rare single gene variant | −0.590 | 0.001 | |
DHCR7 | Syndromic | 0.818 | 0.001 | |
DMD | Genetic association | −0.372 | 0.011 | |
FOXG1 | Syndromic | −0.410 | 0.031 | |
FOXP1 | Rare single gene variant | −0.391 | 0.007 | |
FOXP2 | Rare single gene variant | −1.019 | 0.001 | |
HEPACAM | Rare single gene variant | 0.433 | 0.006 | |
LAMC3 | Rare single gene variant | 0.600 | 0.007 | |
RELN | Genetic association | −0.414 | 0.007 | |
SLC16A3 | Rare single gene variant | 0.912 | 0.006 |