low anterior hairline Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Distance between the hairline (trichion) and the glabella (the most prominent point on the frontal bone above the root of the nose), in the midline, more than two SD below the mean. Alternatively, an apparently decreased distance between the hairline and the glabella. (Human Phenotype Ontology, HP_0000294)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0000294
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Genes

36 genes associated with the low anterior hairline 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
ANKRD11 ankyrin repeat domain 11
ARX aristaless related homeobox
ASXL1 additional sex combs like transcriptional regulator 1
CREBBP CREB binding protein
DOCK6 dedicator of cytokinesis 6
DOCK7 dedicator of cytokinesis 7
FGFR2 fibroblast growth factor receptor 2
FGFR3 fibroblast growth factor receptor 3
HDAC8 histone deacetylase 8
HSPG2 heparan sulfate proteoglycan 2
KCNJ8 potassium channel, inwardly rectifying subfamily J, member 8
LIG4 ligase IV, DNA, ATP-dependent
LRPPRC leucine-rich pentatricopeptide repeat containing
MAN2B1 mannosidase, alpha, class 2B, member 1
NBN nibrin
NIPBL Nipped-B homolog (Drosophila)
NOTCH2 notch 2
NSUN2 NOP2/Sun RNA methyltransferase family, member 2
PEPD peptidase D
POLR1C polymerase (RNA) I polypeptide C, 30kDa
POLR1D polymerase (RNA) I polypeptide D, 16kDa
RAB18 RAB18, member RAS oncogene family
RAB3GAP2 RAB3 GTPase activating protein subunit 2 (non-catalytic)
RAD21 RAD21 homolog (S. pombe)
SLC12A6 solute carrier family 12 (potassium/chloride transporter), member 6
SMARCA2 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 2
SMC1A structural maintenance of chromosomes 1A
SMC3 structural maintenance of chromosomes 3
TBC1D20 TBC1 domain family, member 20
TCF12 transcription factor 12
TCOF1 Treacher Collins-Franceschetti syndrome 1
TECPR2 tectonin beta-propeller repeat containing 2
TMCO1 transmembrane and coiled-coil domains 1
TWIST1 twist family bHLH transcription factor 1
VPS13B vacuolar protein sorting 13 homolog B (yeast)