thin myocardium compact layer Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description reduced thickness of the outer, dense layer of the myocardium (Mammalian Phenotype Ontology, MP_0004057)
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31 gene mutations causing the thin myocardium compact layer phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ADRBK1 adrenergic, beta, receptor kinase 1
ARID3A AT rich interactive domain 3A (BRIGHT-like)
ATP2A2 ATPase, Ca++ transporting, cardiac muscle, slow twitch 2
CALCRL calcitonin receptor-like
CALR calreticulin
CREBBP CREB binding protein
EGLN1 egl-9 family hypoxia-inducible factor 1
EP300 E1A binding protein p300
FES FES proto-oncogene, tyrosine kinase
FOXP1 forkhead box P1
GATA4 GATA binding protein 4
GJA1 gap junction protein, alpha 1, 43kDa
HEXIM1 hexamethylene bis-acetamide inducible 1
HHEX hematopoietically expressed homeobox
HOPX HOP homeobox
JMJD6 jumonji domain containing 6
MAP3K7 mitogen-activated protein kinase kinase kinase 7
MAPK11 mitogen-activated protein kinase 11
MED1 mediator complex subunit 1
MYCN v-myc avian myelocytomatosis viral oncogene neuroblastoma derived homolog
MYL2 myosin, light chain 2, regulatory, cardiac, slow
NCOA6 nuclear receptor coactivator 6
NODAL nodal growth differentiation factor
NPRL3 nitrogen permease regulator-like 3 (S. cerevisiae)
PPARG peroxisome proliferator-activated receptor gamma
PTPN11 protein tyrosine phosphatase, non-receptor type 11
SPTAN1 spectrin, alpha, non-erythrocytic 1
VCAM1 vascular cell adhesion molecule 1
VEGFA vascular endothelial growth factor A
YWHAE tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein, epsilon
ZFPM2 zinc finger protein, FOG family member 2