abnormality of the tricuspid valve Gene Set
Genes
19 genes associated with the abnormality of the tricuspid valve phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
| Symbol |
Name |
|
ADAMTSL2
|
ADAMTS-like 2
|
|
AGGF1
|
angiogenic factor with G patch and FHA domains 1
|
|
ARVCF
|
armadillo repeat gene deleted in velocardiofacial syndrome
|
|
CCDC22
|
coiled-coil domain containing 22
|
|
CHST3
|
carbohydrate (chondroitin 6) sulfotransferase 3
|
|
COMT
|
catechol-O-methyltransferase
|
|
COX7B
|
cytochrome c oxidase subunit VIIb
|
|
FBN1
|
fibrillin 1
|
|
FLNA
|
filamin A, alpha
|
|
GP1BB
|
glycoprotein Ib (platelet), beta polypeptide
|
|
HCCS
|
holocytochrome c synthase
|
|
HIRA
|
histone cell cycle regulator
|
|
KIAA0196
|
KIAA0196
|
|
MYH7
|
myosin, heavy chain 7, cardiac muscle, beta
|
|
ROR2
|
receptor tyrosine kinase-like orphan receptor 2
|
|
RPS6KA3
|
ribosomal protein S6 kinase, 90kDa, polypeptide 3
|
|
SCN5A
|
sodium channel, voltage gated, type V alpha subunit
|
|
TBX1
|
T-box 1
|
|
UFD1L
|
ubiquitin fusion degradation 1 like (yeast)
|
