full cheeks Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Increased prominence or roundness of soft tissues between zygomata and mandible. (Human Phenotype Ontology, HP_0000293)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0000293
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Genes

57 genes associated with the full cheeks phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
ACTB actin, beta
ACTG1 actin gamma 1
ADAMTSL2 ADAMTS-like 2
AGL amylo-alpha-1, 6-glucosidase, 4-alpha-glucanotransferase
AIP aryl hydrocarbon receptor interacting protein
ASXL1 additional sex combs like transcriptional regulator 1
ATP7A ATPase, Cu++ transporting, alpha polypeptide
B9D1 B9 protein domain 1
B9D2 B9 protein domain 2
BMP2 bone morphogenetic protein 2
BRAF B-Raf proto-oncogene, serine/threonine kinase
CC2D2A coiled-coil and C2 domain containing 2A
CEP290 centrosomal protein 290kDa
CLCF1 cardiotrophin-like cytokine factor 1
CRLF1 cytokine receptor-like factor 1
EDN1 endothelin 1
EFEMP2 EGF containing fibulin-like extracellular matrix protein 2
ELN elastin
EYA1 EYA transcriptional coactivator and phosphatase 1
FBLN5 fibulin 5
FBN1 fibrillin 1
FGF3 fibroblast growth factor 3
FLNA filamin A, alpha
GNAS GNAS complex locus
HRAS Harvey rat sarcoma viral oncogene homolog
HSPG2 heparan sulfate proteoglycan 2
IDUA iduronidase, alpha-L-
IFT122 intraflagellar transport 122
IMPAD1 inositol monophosphatase domain containing 1
KIF11 kinesin family member 11
KRAS Kirsten rat sarcoma viral oncogene homolog
LMNA lamin A/C
MAP2K1 mitogen-activated protein kinase kinase 1
MAP2K2 mitogen-activated protein kinase kinase 2
MKS1 Meckel syndrome, type 1
MOCS1 molybdenum cofactor synthesis 1
MOCS2 molybdenum cofactor synthesis 2
NOTCH2 notch 2
NRAS neuroblastoma RAS viral (v-ras) oncogene homolog
OCRL oculocerebrorenal syndrome of Lowe
PAX1 paired box 1
PCNT pericentrin
PIK3CA phosphatidylinositol-4,5-bisphosphate 3-kinase, catalytic subunit alpha
RPGRIP1 retinitis pigmentosa GTPase regulator interacting protein 1
RPGRIP1L RPGRIP1-like
SH3PXD2B SH3 and PX domains 2B
SHANK3 SH3 and multiple ankyrin repeat domains 3
SIM1 single-minded family bHLH transcription factor 1
SLC26A2 solute carrier family 26 (anion exchanger), member 2
TAZ tafazzin
TCF4 transcription factor 4
TCTN2 tectonic family member 2
TMEM216 transmembrane protein 216
TMEM231 transmembrane protein 231
TMEM67 transmembrane protein 67
WDPCP WD repeat containing planar cell polarity effector
WDR19 WD repeat domain 19