Table 3 Significant nervous system-related categories identified in the disease and functional enrichment analyses using IPA software, considering 40 genes identified in the gene-wide analyses surpassing follow-up significance threshold (P-value < 1e-03).

From: Gene-wide Association Study Reveals RNF122 Ubiquitin Ligase as a Novel Susceptibility Gene for Attention Deficit Hyperactivity Disorder

Super-Categories

Diseases or Functions Categories

P-value

Molecules

Hereditary Disorder, Neurological Disease, Organismal Injury and Abnormalities

autosomal dominant spastic paraplegia type 4

1.85e-03

SPAST

Developmental Disorder, Hereditary Disorder, Neurological Disease, Organismal Injury and Abnormalities

autosomal recessive mental retardation type 39

1.85e-03

TTI2

Developmental Disorder, Neurological Disease, Organismal Injury and Abnormalities

meroanencephaly

1.85e-03

ALX1

Organismal Development

relaxation of mice

5.55e-03

ATP1A1

Connective Tissue Disorders, Developmental Disorder, Neurological Disease, Skeletal and Muscular Disorders

acrania

7.40e-03

ALX1

Cell Morphology, Cellular Assembly and Organization, Cellular Development, Cellular Function and Maintenance, Cellular Growth and Proliferation, Neurological Disease, Organismal Injury and Abnormalities

swelling of neurites

7.40e-03

SPAST

Nervous System Development and Function

antinociception of spinal cord

9.24e-03

GPER1

Cellular Assembly and Organization, Cellular Function and Maintenance, Nervous System Development and Function

axonal transport of vesicles

9.24e-03

SPAST

Nervous System Development and Function

abnormal morphology of nervous system

1.10e-02

ALX1, MAB21L2, PEA15, RAP1B, SPAST, STXBP3

Connective Tissue Disorders, Developmental Disorder, Organismal Development, Skeletal and Muscular Disorders

clefting of face

1.29e-02

ALX1

Embryonic Development, Nervous System Development and Function, Organismal Development, Tissue Morphology

abnormal morphology of neural crest

1.47e-02

NCSTN

Cell Morphology, Nervous System Development and Function, Tissue Morphology

abnormal morphology of neurites

3.92e-02

RAP1B, SPAST

Connective Tissue Development and Function, Organ Morphology, Organismal Development, Skeletal and Muscular System Development and Function, Tissue Development

abnormal morphology of supraoccipital bone

4.00e-02

ALX1

Behavior

addiction behaviour

4.36e-02

ATP1A1

Cell Morphology, Nervous System Development and Function, Neurological Disease, Tissue Morphology

loss of axons

4.89e-02

RAP1B