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. Author manuscript; available in PMC: 2016 May 18.
Published in final edited form as: Mol Psychiatry. 2015 Mar 10;21(1):118–125. doi: 10.1038/mp.2015.17

Table 1.

Many genes reported as deleted in human ASD are downregulated in Ptenm3m4/m3m4 mice at 6-weeks of age. See Supplemental Table 2 for the full list of altered susceptibility genes, their primary references, and differential expression information for the 2-week old cohort.

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