abnormality of femoral epiphysis Gene Set
Genes
28 genes associated with the abnormality of femoral epiphysis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
Symbol |
Name |
ACAN
|
aggrecan
|
ADAMTSL2
|
ADAMTS-like 2
|
CDC6
|
cell division cycle 6
|
CHST3
|
carbohydrate (chondroitin 6) sulfotransferase 3
|
COL10A1
|
collagen, type X, alpha 1
|
COL11A1
|
collagen, type XI, alpha 1
|
COL11A2
|
collagen, type XI, alpha 2
|
COL2A1
|
collagen, type II, alpha 1
|
COMP
|
cartilage oligomeric matrix protein
|
CREBBP
|
CREB binding protein
|
DYM
|
dymeclin
|
GNPTG
|
N-acetylglucosamine-1-phosphate transferase, gamma subunit
|
HSPG2
|
heparan sulfate proteoglycan 2
|
IFT140
|
intraflagellar transport 140
|
IHH
|
indian hedgehog
|
KIF22
|
kinesin family member 22
|
MATN3
|
matrilin 3
|
PCNT
|
pericentrin
|
PLOD3
|
procollagen-lysine, 2-oxoglutarate 5-dioxygenase 3
|
RET
|
ret proto-oncogene
|
SBDS
|
Shwachman-Bodian-Diamond syndrome
|
SLC26A2
|
solute carrier family 26 (anion exchanger), member 2
|
SLC39A13
|
solute carrier family 39 (zinc transporter), member 13
|
SMARCAL1
|
SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a-like 1
|
TBX4
|
T-box 4
|
TRAPPC2
|
trafficking protein particle complex 2
|
TRPS1
|
trichorhinophalangeal syndrome I
|
WISP3
|
WNT1 inducible signaling pathway protein 3
|