ventricular hypoplasia Gene Set
Genes
27 gene mutations causing the ventricular hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
| Symbol |
Name |
|
ADRBK1
|
adrenergic, beta, receptor kinase 1
|
|
BMP10
|
bone morphogenetic protein 10
|
|
CYP51A1
|
cytochrome P450, family 51, subfamily A, polypeptide 1
|
|
EPO
|
erythropoietin
|
|
EPOR
|
erythropoietin receptor
|
|
FGFR2
|
fibroblast growth factor receptor 2
|
|
FOXM1
|
forkhead box M1
|
|
GAB1
|
GRB2-associated binding protein 1
|
|
HAND1
|
heart and neural crest derivatives expressed 1
|
|
LATS2
|
large tumor suppressor kinase 2
|
|
MED1
|
mediator complex subunit 1
|
|
MED24
|
mediator complex subunit 24
|
|
MEF2C
|
myocyte enhancer factor 2C
|
|
MOSPD3
|
motile sperm domain containing 3
|
|
MYH10
|
myosin, heavy chain 10, non-muscle
|
|
NACA
|
nascent polypeptide-associated complex alpha subunit
|
|
NPRL3
|
nitrogen permease regulator-like 3 (S. cerevisiae)
|
|
PARD3
|
par-3 family cell polarity regulator
|
|
PBRM1
|
polybromo 1
|
|
PITX2
|
paired-like homeodomain 2
|
|
PRDM16
|
PR domain containing 16
|
|
RXRA
|
retinoid X receptor, alpha
|
|
SEC24B
|
SEC24 family member B
|
|
SMYD1
|
SET and MYND domain containing 1
|
|
TAB1
|
TGF-beta activated kinase 1/MAP3K7 binding protein 1
|
|
TH
|
tyrosine hydroxylase
|
|
TTN
|
titin
|
