prominent supraorbital ridges Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Greater than average forward and/or lateral protrusion of the supraorbital portion of the frontal bones. (Human Phenotype Ontology, HP_0000336)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0000336
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Genes

22 genes associated with the prominent supraorbital ridges 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
AGPAT2 1-acylglycerol-3-phosphate O-acyltransferase 2
ARX aristaless related homeobox
BSCL2 Berardinelli-Seip congenital lipodystrophy 2 (seipin)
CAV1 caveolin 1, caveolae protein, 22kDa
EDA ectodysplasin A
FBXO31 F-box protein 31
FGFR1 fibroblast growth factor receptor 1
FLNA filamin A, alpha
FOS FBJ murine osteosarcoma viral oncogene homolog
FREM1 FRAS1 related extracellular matrix 1
GRIA3 glutamate receptor, ionotropic, AMPA 3
HDAC8 histone deacetylase 8
KCNJ8 potassium channel, inwardly rectifying subfamily J, member 8
OPHN1 oligophrenin 1
PHF6 PHD finger protein 6
PIK3R1 phosphoinositide-3-kinase, regulatory subunit 1 (alpha)
PITX2 paired-like homeodomain 2
PTH1R parathyroid hormone 1 receptor
SEC23A Sec23 homolog A (S. cerevisiae)
SP7 Sp7 transcription factor
UBE2A ubiquitin-conjugating enzyme E2A