ventricular hypoplasia Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description underdevelopment or reduced size, usually due to a reduced number of cells, of one or both of the two lower chambers of the heart (Mammalian Phenotype Ontology, MP_0000279)
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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