sparse eyebrow Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Decreased density/number and/or decreased diameter of eyebrow hairs. (Human Phenotype Ontology, HP_0000535)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0000535
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Genes

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

Symbol Name
BANF1 barrier to autointegration factor 1
CDH3 cadherin 3, type 1, P-cadherin (placental)
CHST3 carbohydrate (chondroitin 6) sulfotransferase 3
DOLK dolichol kinase
DSG4 desmoglein 4
DSP desmoplakin
EBP emopamil binding protein (sterol isomerase)
EDA ectodysplasin A
EDAR ectodysplasin A receptor
FIG4 FIG4 phosphoinositide 5-phosphatase
GJB2 gap junction protein, beta 2, 26kDa
GJB6 gap junction protein, beta 6, 30kDa
GNPTAB N-acetylglucosamine-1-phosphate transferase, alpha and beta subunits
HR hair growth associated
IRX5 iroquois homeobox 5
KDM6A lysine (K)-specific demethylase 6A
KMT2D lysine (K)-specific methyltransferase 2D
KRT17 keratin 17, type I
LIG4 ligase IV, DNA, ATP-dependent
LIPH lipase, member H
LPAR6 lysophosphatidic acid receptor 6
MBTPS2 membrane-bound transcription factor peptidase, site 2
MEGF8 multiple EGF-like-domains 8
NAA10 N(alpha)-acetyltransferase 10, NatA catalytic subunit
NSUN2 NOP2/Sun RNA methyltransferase family, member 2
PQBP1 polyglutamine binding protein 1
PVRL1 poliovirus receptor-related 1 (herpesvirus entry mediator C)
PVRL4 poliovirus receptor-related 4
RIN2 Ras and Rab interactor 2
RMRP RNA component of mitochondrial RNA processing endoribonuclease
RNU4ATAC RNA, U4atac small nuclear (U12-dependent splicing)
SAT1 spermidine/spermine N1-acetyltransferase 1
SOS1 son of sevenless homolog 1 (Drosophila)
SPINK5 serine peptidase inhibitor, Kazal type 5
ST14 suppression of tumorigenicity 14 (colon carcinoma)
TBX3 T-box 3
TMCO1 transmembrane and coiled-coil domains 1
TP63 tumor protein p63
TRPS1 trichorhinophalangeal syndrome I
TWIST2 twist family bHLH transcription factor 2
WNT10A wingless-type MMTV integration site family, member 10A