posterior embryotoxon Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description A posterior embryotoxon is the presence of a prominent and anteriorly displaced line of Schwalbe. (Human Phenotype Ontology, HP_0000627)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0000627
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Genes

30 genes associated with the posterior embryotoxon phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
BAZ1B bromodomain adjacent to zinc finger domain, 1B
CLIP2 CAP-GLY domain containing linker protein 2
COX7B cytochrome c oxidase subunit VIIb
ELN elastin
FOXC1 forkhead box C1
GTF2I general transcription factor IIi
GTF2IRD1 GTF2I repeat domain containing 1
HCCS holocytochrome c synthase
JAG1 jagged 1
LIMK1 LIM domain kinase 1
PEX1 peroxisomal biogenesis factor 1
PEX10 peroxisomal biogenesis factor 10
PEX11B peroxisomal biogenesis factor 11 beta
PEX12 peroxisomal biogenesis factor 12
PEX13 peroxisomal biogenesis factor 13
PEX14 peroxisomal biogenesis factor 14
PEX16 peroxisomal biogenesis factor 16
PEX19 peroxisomal biogenesis factor 19
PEX2 peroxisomal biogenesis factor 2
PEX26 peroxisomal biogenesis factor 26
PEX3 peroxisomal biogenesis factor 3
PEX5 peroxisomal biogenesis factor 5
PEX6 peroxisomal biogenesis factor 6
PIK3R1 phosphoinositide-3-kinase, regulatory subunit 1 (alpha)
PITX2 paired-like homeodomain 2
RFC2 replication factor C (activator 1) 2, 40kDa
SLC38A8 solute carrier family 38, member 8
TBL2 transducin (beta)-like 2
TBX1 T-box 1
YAP1 Yes-associated protein 1
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