myocardial fiber degeneration Gene Set
Genes
24 gene mutations causing the myocardial fiber degeneration phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
Symbol |
Name |
ABCA5
|
ATP-binding cassette, sub-family A (ABC1), member 5
|
ACADM
|
acyl-CoA dehydrogenase, C-4 to C-12 straight chain
|
ACADVL
|
acyl-CoA dehydrogenase, very long chain
|
ACKR3
|
atypical chemokine receptor 3
|
ACTC1
|
actin, alpha, cardiac muscle 1
|
BAG3
|
BCL2-associated athanogene 3
|
BCL6
|
B-cell CLL/lymphoma 6
|
CHD2
|
chromodomain helicase DNA binding protein 2
|
COX1
|
|
DES
|
desmin
|
DMD
|
dystrophin
|
DTNA
|
dystrobrevin, alpha
|
HIF3A
|
hypoxia inducible factor 3, alpha subunit
|
IGHMBP2
|
immunoglobulin mu binding protein 2
|
LAMA4
|
laminin, alpha 4
|
LMNA
|
lamin A/C
|
MPZL3
|
myelin protein zero-like 3
|
PPARA
|
peroxisome proliferator-activated receptor alpha
|
PTCD2
|
pentatricopeptide repeat domain 2
|
SCN8A
|
sodium channel, voltage gated, type VIII alpha subunit
|
SOS1
|
son of sevenless homolog 1 (Drosophila)
|
TREX1
|
three prime repair exonuclease 1
|
TRIM54
|
tripartite motif containing 54
|
VEGFA
|
vascular endothelial growth factor A
|