disorganized myocardium Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description derangement of the pattern cardiac muscle layers (Mammalian Phenotype Ontology, MP_0002190)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0002190
Similar Terms
Downloads & Tools

Genes

30 gene mutations causing the disorganized myocardium phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ABI1 abl-interactor 1
ABL1 ABL proto-oncogene 1, non-receptor tyrosine kinase
ACTC1 actin, alpha, cardiac muscle 1
ADM adrenomedullin
ADRBK1 adrenergic, beta, receptor kinase 1
BIN1 bridging integrator 1
CALCRL calcitonin receptor-like
DES desmin
FOXH1 forkhead box H1
FOXM1 forkhead box M1
FOXP1 forkhead box P1
FXR1 fragile X mental retardation, autosomal homolog 1
HIF1A hypoxia inducible factor 1, alpha subunit (basic helix-loop-helix transcription factor)
HTR2B 5-hydroxytryptamine (serotonin) receptor 2B, G protein-coupled
IGF2R insulin-like growth factor 2 receptor
MORF4L1 mortality factor 4 like 1
MYBPC3 myosin binding protein C, cardiac
MYH6 myosin, heavy chain 6, cardiac muscle, alpha
NCOA6 nuclear receptor coactivator 6
NF1 neurofibromin 1
NKX2-5 NK2 homeobox 5
NOTCH1 notch 1
PDGFRB platelet-derived growth factor receptor, beta polypeptide
RBPJ recombination signal binding protein for immunoglobulin kappa J region
RYR2 ryanodine receptor 2 (cardiac)
SALL4 spalt-like transcription factor 4
SRSF10 serine/arginine-rich splicing factor 10
TGM2 transglutaminase 2
VCAM1 vascular cell adhesion molecule 1
XIRP2 xin actin binding repeat containing 2