heart hypoplasia Gene Set
Genes
16 gene mutations causing the heart hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
| Symbol |
Name |
|
ACVRL1
|
activin A receptor type II-like 1
|
|
ADRBK1
|
adrenergic, beta, receptor kinase 1
|
|
CYP51A1
|
cytochrome P450, family 51, subfamily A, polypeptide 1
|
|
FGF16
|
fibroblast growth factor 16
|
|
FGF9
|
fibroblast growth factor 9
|
|
FGFR1
|
fibroblast growth factor receptor 1
|
|
ITPA
|
inosine triphosphatase (nucleoside triphosphate pyrophosphatase)
|
|
MED1
|
mediator complex subunit 1
|
|
MED24
|
mediator complex subunit 24
|
|
NCOA6
|
nuclear receptor coactivator 6
|
|
NF1
|
neurofibromin 1
|
|
NOTCH2
|
notch 2
|
|
POFUT1
|
protein O-fucosyltransferase 1
|
|
TBX20
|
T-box 20
|
|
TCEB3
|
transcription elongation factor B (SIII), polypeptide 3 (110kDa, elongin A)
|
|
WNK1
|
WNK lysine deficient protein kinase 1
|
