Neurobehavioral Manifestations Gene Set

Dataset dbGAP Gene-Trait Associations
Category disease or phenotype associations
Type trait
Description Signs and symptoms of higher cortical dysfunction caused by organic conditions. These include certain behavioral alterations and impairments of skills involved in the acquisition, processing, and utilization of knowledge or information. (Experimental Factor Ontology, EFO_0004364)
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Genes

9 genes associated with the trait Neurobehavioral Manifestations in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset.

Symbol Name Standardized Value
ATRNL1 attractin-like 1 0.443956
TMEM245 transmembrane protein 245 0.443956
DCDC2 doublecortin domain containing 2 0.406869
CRTC3 CREB regulated transcription coactivator 3 0.406869
PKNOX1 PBX/knotted 1 homeobox 1 0.33862
C20ORF196 chromosome 20 open reading frame 196 0.310838
KCTD2 potassium channel tetramerization domain containing 2 0.310838
MYRIP myosin VIIA and Rab interacting protein 0.29992
FAM110C family with sequence similarity 110, member C 0.29992