sloping forehead Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Inclination of the anterior surface of the forehead from the vertical more than two standard deviations above the mean (objective); or apparently excessive posterior sloping of the forehead in a lateral view. (Human Phenotype Ontology, HP_0000340)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0000340
Similar Terms
Downloads & Tools

Genes

76 genes associated with the sloping forehead 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
ASNS asparagine synthetase (glutamine-hydrolyzing)
ASPM asp (abnormal spindle) homolog, microcephaly associated (Drosophila)
ATR ATR serine/threonine kinase
B9D1 B9 protein domain 1
B9D2 B9 protein domain 2
BRCA2 breast cancer 2, early onset
BRIP1 BRCA1 interacting protein C-terminal helicase 1
BUB1 BUB1 mitotic checkpoint serine/threonine kinase
BUB1B BUB1 mitotic checkpoint serine/threonine kinase B
BUB3 BUB3 mitotic checkpoint protein
CC2D2A coiled-coil and C2 domain containing 2A
CDK5RAP2 CDK5 regulatory subunit associated protein 2
CEP135 centrosomal protein 135kDa
CEP152 centrosomal protein 152kDa
CEP290 centrosomal protein 290kDa
CEP57 centrosomal protein 57kDa
CPT2 carnitine palmitoyltransferase 2
CTSD cathepsin D
DDX11 DEAD/H (Asp-Glu-Ala-Asp/His) box helicase 11
DYM dymeclin
EMG1 EMG1 N1-specific pseudouridine methyltransferase
ERCC4 excision repair cross-complementation group 4
ERCC6 excision repair cross-complementation group 6
FANCA Fanconi anemia, complementation group A
FANCB Fanconi anemia, complementation group B
FANCC Fanconi anemia, complementation group C
FANCD2 Fanconi anemia, complementation group D2
FANCE Fanconi anemia, complementation group E
FANCF Fanconi anemia, complementation group F
FANCG Fanconi anemia, complementation group G
FANCI Fanconi anemia, complementation group I
FANCL Fanconi anemia, complementation group L
FANCM Fanconi anemia, complementation group M
GLI3 GLI family zinc finger 3
KAT6B K(lysine) acetyltransferase 6B
KIF11 kinesin family member 11
KIF1BP KIF1 binding protein
KIF7 kinesin family member 7
LIG4 ligase IV, DNA, ATP-dependent
LTBP4 latent transforming growth factor beta binding protein 4
MCPH1 microcephalin 1
MGP matrix Gla protein
MKS1 Meckel syndrome, type 1
NBN nibrin
NDE1 nudE neurodevelopment protein 1
NHEJ1 nonhomologous end-joining factor 1
NSUN2 NOP2/Sun RNA methyltransferase family, member 2
OCLN occludin
PALB2 partner and localizer of BRCA2
PCNT pericentrin
PHGDH phosphoglycerate dehydrogenase
PSAT1 phosphoserine aminotransferase 1
QARS glutaminyl-tRNA synthetase
RAD51C RAD51 paralog C
RELN reelin
RNU4ATAC RNA, U4atac small nuclear (U12-dependent splicing)
RPGRIP1 retinitis pigmentosa GTPase regulator interacting protein 1
RPGRIP1L RPGRIP1-like
RUNX2 runt-related transcription factor 2
SC5D sterol-C5-desaturase
SETBP1 SET binding protein 1
SLC25A19 solute carrier family 25 (mitochondrial thiamine pyrophosphate carrier), member 19
SLX4 SLX4 structure-specific endonuclease subunit
STAMBP STAM binding protein
TCTN2 tectonic family member 2
TMEM216 transmembrane protein 216
TMEM231 transmembrane protein 231
TMEM67 transmembrane protein 67
TTI2 TELO2 interacting protein 2
TUBGCP6 tubulin, gamma complex associated protein 6
VIPAS39 VPS33B interacting protein, apical-basolateral polarity regulator, spe-39 homolog
VPS33B vacuolar protein sorting 33 homolog B (yeast)
WDPCP WD repeat containing planar cell polarity effector
WDR62 WD repeat domain 62
ZNF335 zinc finger protein 335