narrow palate Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Width of the palate more than 2 SD below the mean (objective) or apparently decreased palatal width (subjective). (Human Phenotype Ontology, HP_0000189)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0000189
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Genes

26 genes associated with the narrow palate phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
ADAMTS10 ADAM metallopeptidase with thrombospondin type 1 motif, 10
ASXL1 additional sex combs like transcriptional regulator 1
CCBE1 collagen and calcium binding EGF domains 1
CPT2 carnitine palmitoyltransferase 2
CREBBP CREB binding protein
CTSK cathepsin K
DPM1 dolichyl-phosphate mannosyltransferase polypeptide 1, catalytic subunit
EP300 E1A binding protein p300
FBN1 fibrillin 1
FGFR2 fibroblast growth factor receptor 2
HERC2 HECT and RLD domain containing E3 ubiquitin protein ligase 2
KANSL1 KAT8 regulatory NSL complex subunit 1
MED12 mediator complex subunit 12
MEGF8 multiple EGF-like-domains 8
NSD1 nuclear receptor binding SET domain protein 1
RAB18 RAB18, member RAS oncogene family
RARS2 arginyl-tRNA synthetase 2, mitochondrial
RPS6KA3 ribosomal protein S6 kinase, 90kDa, polypeptide 3
RUNX2 runt-related transcription factor 2
SKI SKI proto-oncogene
SMS spermine synthase
TRPS1 trichorhinophalangeal syndrome I
TWIST1 twist family bHLH transcription factor 1
VPS13B vacuolar protein sorting 13 homolog B (yeast)
WNT5A wingless-type MMTV integration site family, member 5A
WNT7A wingless-type MMTV integration site family, member 7A