broad phalanges of the hand Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Increased width of the phalanges of the hand. (Human Phenotype Ontology, HP_0009768)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0009768
Similar Terms
Downloads & Tools

Genes

32 genes associated with the broad phalanges of the hand phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
ACAN aggrecan
ADAMTS10 ADAM metallopeptidase with thrombospondin type 1 motif, 10
B3GALT6 UDP-Gal:betaGal beta 1,3-galactosyltransferase polypeptide 6
B3GAT3 beta-1,3-glucuronyltransferase 3
COL10A1 collagen, type X, alpha 1
COL2A1 collagen, type II, alpha 1
CREBBP CREB binding protein
EP300 E1A binding protein p300
EZH2 enhancer of zeste 2 polycomb repressive complex 2 subunit
FBN1 fibrillin 1
FGFR1 fibroblast growth factor receptor 1
FGFR2 fibroblast growth factor receptor 2
FLNA filamin A, alpha
FLNB filamin B, beta
G6PC3 glucose 6 phosphatase, catalytic, 3
GLI3 GLI family zinc finger 3
GPC3 glypican 3
HOXD13 homeobox D13
IFT122 intraflagellar transport 122
KIF22 kinesin family member 22
MED12 mediator complex subunit 12
MEGF8 multiple EGF-like-domains 8
NOG noggin
RBM8A RNA binding motif protein 8A
ROR2 receptor tyrosine kinase-like orphan receptor 2
SALL1 spalt-like transcription factor 1
SNIP1 Smad nuclear interacting protein 1
SUMF1 sulfatase modifying factor 1
USP9X ubiquitin specific peptidase 9, X-linked
WDR19 WD repeat domain 19
WNT5A wingless-type MMTV integration site family, member 5A
XYLT1 xylosyltransferase I