thick eyebrow Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Increased density/number and/or increased diameter of eyebrow hairs. (Human Phenotype Ontology, HP_0000574)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0000574
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Genes

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

Symbol Name
ABCA5 ATP-binding cassette, sub-family A (ABC1), member 5
ABCC9 ATP-binding cassette, sub-family C (CFTR/MRP), member 9
ANKRD11 ankyrin repeat domain 11
ARID1A AT rich interactive domain 1A (SWI-like)
ARID1B AT rich interactive domain 1B (SWI1-like)
B3GAT3 beta-1,3-glucuronyltransferase 3
BCOR BCL6 corepressor
CCDC8 coiled-coil domain containing 8
CREBBP CREB binding protein
CUL7 cullin 7
DOCK7 dedicator of cytokinesis 7
EXT1 exostosin glycosyltransferase 1
FAM20A family with sequence similarity 20, member A
FBXL4 F-box and leucine-rich repeat protein 4
FBXO31 F-box protein 31
FUCA1 fucosidase, alpha-L- 1, tissue
GNS glucosamine (N-acetyl)-6-sulfatase
HDAC8 histone deacetylase 8
HMGA2 high mobility group AT-hook 2
IDUA iduronidase, alpha-L-
KCNJ8 potassium channel, inwardly rectifying subfamily J, member 8
KCNK9 potassium channel, two pore domain subfamily K, member 9
KIF1BP KIF1 binding protein
KMT2A lysine (K)-specific methyltransferase 2A
LEMD3 LEM domain containing 3
MAN2B1 mannosidase, alpha, class 2B, member 1
MBD5 methyl-CpG binding domain protein 5
MEF2C myocyte enhancer factor 2C
MGAT2 mannosyl (alpha-1,6-)-glycoprotein beta-1,2-N-acetylglucosaminyltransferase
NBAS neuroblastoma amplified sequence
NFIX nuclear factor I/X (CCAAT-binding transcription factor)
NIPBL Nipped-B homolog (Drosophila)
NOTCH2 notch 2
NSUN2 NOP2/Sun RNA methyltransferase family, member 2
OBSL1 obscurin-like 1
PAX3 paired box 3
PHF6 PHD finger protein 6
RAD21 RAD21 homolog (S. pombe)
RET ret proto-oncogene
RPS6KA3 ribosomal protein S6 kinase, 90kDa, polypeptide 3
SHANK3 SH3 and multiple ankyrin repeat domains 3
SLC35A2 solute carrier family 35 (UDP-galactose transporter), member A2
SLC9A6 solute carrier family 9, subfamily A (NHE6, cation proton antiporter 6), member 6
SMAD4 SMAD family member 4
SMARCA4 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 4
SMARCB1 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily b, member 1
SMARCE1 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily e, member 1
SMC1A structural maintenance of chromosomes 1A
SMC3 structural maintenance of chromosomes 3
SOX11 SRY (sex determining region Y)-box 11
SUMF1 sulfatase modifying factor 1
TFAP2B transcription factor AP-2 beta (activating enhancer binding protein 2 beta)
TMCO1 transmembrane and coiled-coil domains 1
TP63 tumor protein p63
TRPS1 trichorhinophalangeal syndrome I
VPS13B vacuolar protein sorting 13 homolog B (yeast)