long eyelashes Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Mid upper eyelash length >10 mm or increased length of the eyelashes (subjective). (Human Phenotype Ontology, HP_0000527)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0000527
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Genes

25 genes associated with the long eyelashes phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
ABCC9 ATP-binding cassette, sub-family C (CFTR/MRP), member 9
ARID1A AT rich interactive domain 1A (SWI-like)
BMP1 bone morphogenetic protein 1
CLP1 cleavage and polyadenylation factor I subunit 1
CREBBP CREB binding protein
EP300 E1A binding protein p300
FBN1 fibrillin 1
FGF5 fibroblast growth factor 5
HDAC8 histone deacetylase 8
HSPG2 heparan sulfate proteoglycan 2
KDM6A lysine (K)-specific demethylase 6A
KMT2A lysine (K)-specific methyltransferase 2A
MGAT2 mannosyl (alpha-1,6-)-glycoprotein beta-1,2-N-acetylglucosaminyltransferase
MOGS mannosyl-oligosaccharide glucosidase
NIPBL Nipped-B homolog (Drosophila)
NOTCH2 notch 2
ORC1 origin recognition complex, subunit 1
ROR2 receptor tyrosine kinase-like orphan receptor 2
SHANK3 SH3 and multiple ankyrin repeat domains 3
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
SMC3 structural maintenance of chromosomes 3
SRCAP Snf2-related CREBBP activator protein
TMCO1 transmembrane and coiled-coil domains 1
WNT5A wingless-type MMTV integration site family, member 5A