abnormality of the metopic suture Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description The frontal suture divides the two halves of the frontal bone of the skull in infants and children and generally undergoes fusion by the age of six. A persistent frontal suture is referred to as a metopic suture. (Human Phenotype Ontology, HP_0005556)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0005556
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Genes

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

Symbol Name
ABCC8 ATP-binding cassette, sub-family C (CFTR/MRP), member 8
ACTB actin, beta
ACTG1 actin gamma 1
ADSL adenylosuccinate lyase
ASXL1 additional sex combs like transcriptional regulator 1
CDC6 cell division cycle 6
ERCC1 excision repair cross-complementation group 1
ERCC2 excision repair cross-complementation group 2
ERCC5 excision repair cross-complementation group 5
ERCC6 excision repair cross-complementation group 6
FOXG1 forkhead box G1
GCK glucokinase (hexokinase 4)
GLI3 GLI family zinc finger 3
INS insulin
KANSL1 KAT8 regulatory NSL complex subunit 1
KCNJ11 potassium channel, inwardly rectifying subfamily J, member 11
SC5D sterol-C5-desaturase
SETBP1 SET binding protein 1