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