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Table 2 Genes involved in ASD, SZ, ID, and eye disorders that overlap with the 319 nominal DEGs. Two additional genes were included based on literature support: MEIS1 is a glaucoma candidate that is not in the NEI/NIH eye database, and SPON1 is not in any of the SZ candidate gene databases, but was recently identified in an exome sequencing study (both denoted by asterisk *). Genes shown in bold type are the DEGs at padj < 0.1

From: Transcriptome analysis of neural progenitor cells derived from Lowe syndrome induced pluripotent stem cells: identification of candidate genes for the neurodevelopmental and eye manifestations

ASD

SZ

IDD

EYE

AFF2

BMP6

AFF2

CNGB1

ANO5

CA8

CA8

COL2A1

CA8

CACNA1C

EEF1A2

EFEMP1

CACNA1C

CHN2

MLC1

MEIS2*

CADPS2

CHRFAM7A

RELN

PITX2

COMT

COMT

TH

SPON1*

DNAH3

MLC1

XYLT1

TNFRSF11B

DNER

PCDHA6

  

DPP10

PNPO

  

DPP6

PPP1R16B

  

EEF1A2

PROZ

  

GABRG3

RELN

  

GALNT10

SLC1A3

  

GDA

SNCG

  

KCND3

SPON1*

  

KCNJ12

TH

  

MEIS2

ADCY2

  

OTX1

   

PCDHA6

   

RELN

   

RORA

   

SYT17

   

ZNF385B

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