abnormality of the antihelix Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description An abnormality of the antihelix. (Human Phenotype Ontology, HP_0009738)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0009738
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Genes

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

Symbol Name
AP4E1 adaptor-related protein complex 4, epsilon 1 subunit
CHD7 chromodomain helicase DNA binding protein 7
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
FGF10 fibroblast growth factor 10
FGFR2 fibroblast growth factor receptor 2
FGFR3 fibroblast growth factor receptor 3
FIG4 FIG4 phosphoinositide 5-phosphatase
FLNA filamin A, alpha
FOXG1 forkhead box G1
GLI2 GLI family zinc finger 2
KAT6B K(lysine) acetyltransferase 6B
KCTD1 potassium channel tetramerization domain containing 1
LIG4 ligase IV, DNA, ATP-dependent
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)
RBM10 RNA binding motif protein 10
SALL1 spalt-like transcription factor 1
SEMA3E sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3E
SLC16A2 solute carrier family 16, member 2 (thyroid hormone transporter)