Abnormality Of The Antihelix Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description An abnormality of the antihelix. (Human Phenotype Ontology, HP_0009738)
External Link https://www.disgenet.org/browser/0/1/0/C4021395
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Genes

17 genes associated with the disease Abnormality Of The Antihelix in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
EFTUD2 elongation factor Tu GTP binding domain containing 2
EVC Ellis van Creveld protein
EVC2 Ellis van Creveld syndrome 2
EYA1 EYA transcriptional coactivator and phosphatase 1
FGFR2 fibroblast growth factor receptor 2
FGFR3 fibroblast growth factor receptor 3
FOXG1 forkhead box G1
KAT6B K(lysine) acetyltransferase 6B
KCTD1 potassium channel tetramerization domain containing 1
LIG4 ligase IV, DNA, ATP-dependent
MECP2 methyl CpG binding protein 2
NSUN2 NOP2/Sun RNA methyltransferase family, member 2
PAX1 paired box 1
RAB3GAP1 RAB3 GTPase activating protein subunit 1 (catalytic)
RAB3GAP2 RAB3 GTPase activating protein subunit 2 (non-catalytic)
TWIST1 twist family bHLH transcription factor 1
XYLT2 xylosyltransferase II