congenital hip dislocation Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0001374
Similar Terms
Downloads & Tools

Genes

28 genes associated with the congenital hip dislocation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
ACTA1 actin, alpha 1, skeletal muscle
ALDH18A1 aldehyde dehydrogenase 18 family, member A1
ATP6V0A2 ATPase, H+ transporting, lysosomal V0 subunit a2
CHRM3 cholinergic receptor, muscarinic 3
COL1A1 collagen, type I, alpha 1
COL1A2 collagen, type I, alpha 2
DHODH dihydroorotate dehydrogenase (quinone)
EYA1 EYA transcriptional coactivator and phosphatase 1
FLNA filamin A, alpha
HSPG2 heparan sulfate proteoglycan 2
KAT6B K(lysine) acetyltransferase 6B
KIF22 kinesin family member 22
KMT2D lysine (K)-specific methyltransferase 2D
MKKS McKusick-Kaufman syndrome
NSDHL NAD(P) dependent steroid dehydrogenase-like
OFD1 oral-facial-digital syndrome 1
PIEZO2 piezo-type mechanosensitive ion channel component 2
PORCN porcupine homolog (Drosophila)
PYCR1 pyrroline-5-carboxylate reductase 1
RECQL4 RecQ protein-like 4
RYR1 ryanodine receptor 1 (skeletal)
SEPN1 selenoprotein N, 1
THRA thyroid hormone receptor, alpha
TPM2 tropomyosin 2 (beta)
TPM3 tropomyosin 3
UBE3B ubiquitin protein ligase E3B
WNT7A wingless-type MMTV integration site family, member 7A
ZNF469 zinc finger protein 469