Table 2 Differentially expressed genes associated with human diseases

rx2

Retinal homeobox gene 2

8.01

2.57E-264

611038

Microphthalmia, isolated 3 (MCOP3)

vsx2

Visual system homeobox 2

4.72

2.81E-122

610092

Microphthalmia, isolated, with coloboma 3 (MCOPCB3)

610093

Microphthalmia, isolated 2 (MCOP2)

hmx1

H6 homeo box 1

2.36

4.45E-55

612109

Oculoauricular syndrome

aldh1a3

Aldehyde dehydrogenase 1 family, member A3

2.33

1.23E-22

610093

Microphthalmia, isolated 8 (MCOP8)

six6b

Sine oculis-related homeobox 6b

1.70

2.72E-04

212550

Microphthalmia, isolated, with cataract 2 (MCOPCT2)

rx3

Retinal homeobox gene 3

0.65

1.08E-18

611038

Microphthalmia, isolated 3 (MCOP3)

arx

Aristaless related homeobox

-0.88

8.28E-28

300004

Corpus callosum, agenesis of, with abnormal genitalia

300215

Lissencephaly, x-linked, 2 (LISX2)

300419

Mental retardation, x-linked, with or without seizures, ARX-related

308350

Epileptic encephalopathy, early infantile, 1 (EIEE1)

309510

Partington x-linked mental retardation syndrome (PRTS)

foxg1a

Forkhead box G1a

-1.23

8.14E-139

613454

Rett syndrome, congenital variant