hip contracture Gene Set
Genes
16 genes associated with the hip contracture phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
| Symbol |
Name |
|
BICD2
|
bicaudal D homolog 2 (Drosophila)
|
|
COL2A1
|
collagen, type II, alpha 1
|
|
ESCO2
|
establishment of sister chromatid cohesion N-acetyltransferase 2
|
|
FBN2
|
fibrillin 2
|
|
HSPG2
|
heparan sulfate proteoglycan 2
|
|
KAT6B
|
K(lysine) acetyltransferase 6B
|
|
MMP2
|
matrix metallopeptidase 2
|
|
MYH3
|
myosin, heavy chain 3, skeletal muscle, embryonic
|
|
PTH1R
|
parathyroid hormone 1 receptor
|
|
RNU4ATAC
|
RNA, U4atac small nuclear (U12-dependent splicing)
|
|
SLC26A2
|
solute carrier family 26 (anion exchanger), member 2
|
|
SPEG
|
SPEG complex locus
|
|
TNNT1
|
troponin T type 1 (skeletal, slow)
|
|
TPM2
|
tropomyosin 2 (beta)
|
|
TRPV4
|
transient receptor potential cation channel, subfamily V, member 4
|
|
ZBTB20
|
zinc finger and BTB domain containing 20
|
