patellar dislocation Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description The kneecap normally is located within the groove termed trochlea on the distal femur and can slide up and down in it. Patellar dislocation occurs if the patella fully dislocates out of the groove. (Human Phenotype Ontology, HP_0002999)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0002999
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Genes

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

Symbol Name
ARVCF armadillo repeat gene deleted in velocardiofacial syndrome
BAZ1B bromodomain adjacent to zinc finger domain, 1B
CANT1 calcium activated nucleotidase 1
CLIP2 CAP-GLY domain containing linker protein 2
COMT catechol-O-methyltransferase
CREBBP CREB binding protein
EBP emopamil binding protein (sterol isomerase)
ELN elastin
FBN2 fibrillin 2
FLNA filamin A, alpha
GDF5 growth differentiation factor 5
GP1BB glycoprotein Ib (platelet), beta polypeptide
GTF2I general transcription factor IIi
GTF2IRD1 GTF2I repeat domain containing 1
HIRA histone cell cycle regulator
IMPAD1 inositol monophosphatase domain containing 1
KAT6B K(lysine) acetyltransferase 6B
LIMK1 LIM domain kinase 1
LMX1B LIM homeobox transcription factor 1, beta
NOTCH2 notch 2
OCRL oculocerebrorenal syndrome of Lowe
RBM8A RNA binding motif protein 8A
RFC2 replication factor C (activator 1) 2, 40kDa
TBL2 transducin (beta)-like 2
TBX1 T-box 1
TBX4 T-box 4
UFD1L ubiquitin fusion degradation 1 like (yeast)
XYLT1 xylosyltransferase I