abnormality of the sella turcica Gene Set

Dataset	HPO Gene-Disease Associations
Category	disease or phenotype associations
Type	phenotype
Description	Abnormality of the sella turcica, a saddle-shaped depression in the sphenoid bone at the base of the human skull. (Human Phenotype Ontology, HP_0002679)
External Link	http://compbio.charite.de/hpoweb/showterm?id=HP:0002679
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Genes

18 genes associated with the abnormality of the sella turcica phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol	Name
ABCC9	ATP-binding cassette, sub-family C (CFTR/MRP), member 9
ADAMTSL2	ADAMTS-like 2
BMP4	bone morphogenetic protein 4
DYM	dymeclin
GNPTAB	N-acetylglucosamine-1-phosphate transferase, alpha and beta subunits
GUSB	glucuronidase, beta
IDUA	iduronidase, alpha-L-
LHX4	LIM homeobox 4
NOTCH2	notch 2
PCNT	pericentrin
PLOD3	procollagen-lysine, 2-oxoglutarate 5-dioxygenase 3
PTCH1	patched 1
PTCH2	patched 2
RMRP	RNA component of mitochondrial RNA processing endoribonuclease
SLC17A5	solute carrier family 17 (acidic sugar transporter), member 5
SUFU	suppressor of fused homolog (Drosophila)
TRIM37	tripartite motif containing 37
ZSWIM6	zinc finger, SWIM-type containing 6