Pica Gene Set

Dataset	CTD Gene-Disease Associations
Category	disease or phenotype associations
Type	disease
Description	An appetite for and the persistent ingestion of non-food substances such as clay. In order to diagnose pica, this behavior must have persisted over a period of at least one month. (Human Phenotype Ontology, HP_0011856)
External Link	http://ctdbase.org/detail.go?type=disease&acc=MESH:D010842
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Genes

13 genes/proteins associated with the disease Pica from the curated CTD Gene-Disease Associations dataset.

Symbol	Name	Standardized Value
FOS	FBJ murine osteosarcoma viral oncogene homolog	1.48273
CYP3A4	cytochrome P450, family 3, subfamily A, polypeptide 4	1.35299
ABCB1	ATP-binding cassette, sub-family B (MDR/TAP), member 1	1.31656
IL6	interleukin 6	1.21076
BDNF	brain-derived neurotrophic factor	1.16335
CASP3	caspase 3, apoptosis-related cysteine peptidase	1.10942
CASP1	caspase 1, apoptosis-related cysteine peptidase	1.08584
TAP1	transporter 1, ATP-binding cassette, sub-family B (MDR/TAP)	1.05423
TYMP	thymidine phosphorylase	1.04978
CEBPB	CCAAT/enhancer binding protein (C/EBP), beta	1.03789
MYC	v-myc avian myelocytomatosis viral oncogene homolog	1.02671
SAT1	spermidine/spermine N1-acetyltransferase 1	1.02151
TP53	tumor protein p53	1.01852