sparse lateral eyebrow Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Decreased density/number and/or decreased diameter of lateral eyebrow hairs. (Human Phenotype Ontology, HP_0005338)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0005338
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Genes

10 genes associated with the sparse lateral eyebrow phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
IRX5 iroquois homeobox 5
KDM6A lysine (K)-specific demethylase 6A
KMT2D lysine (K)-specific methyltransferase 2D
LIG4 ligase IV, DNA, ATP-dependent
NSUN2 NOP2/Sun RNA methyltransferase family, member 2
PQBP1 polyglutamine binding protein 1
PVRL1 poliovirus receptor-related 1 (herpesvirus entry mediator C)
TBX3 T-box 3
TRPS1 trichorhinophalangeal syndrome I
TWIST2 twist family bHLH transcription factor 2