prominent metopic ridge Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Vertical bony ridge positioned in the midline of the forehead. (Human Phenotype Ontology, HP_0005487)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0005487
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Genes

16 genes associated with the prominent metopic ridge 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)
INS insulin
KANSL1 KAT8 regulatory NSL complex subunit 1
KCNJ11 potassium channel, inwardly rectifying subfamily J, member 11
SC5D sterol-C5-desaturase