Table 1.
LVNC related genes.
| Location | Phenotype | Phenotype MIM Number | Gene/Locus |
Gene/Lócus MIM
Number |
Mode of Inheritance |
|---|---|---|---|---|---|
| 14q11.2 | Left ventricular noncompaction [5] | 613426 | MYH7 | 160760 | Autosomal dominant |
| 11p11.2 | Left ventricular noncompaction [10] | 615396 | MYBPC3 | 600958 | Autosomal dominant |
| 11p11.2 | Left ventricular noncompaction [10] | 615396 | MYBPC3 | 600958 | Autosomal dominant |
| 15q22.2 | Left ventricular noncompaction [9] | 611878 | TPM1 | 191010 | — |
| 15q14 | Left ventricular noncompaction [4] | 613424 | ACTC1 | 102540 | Autosomal dominant |
| 1q32.1 | Left ventricular noncompaction [6] | 601494 | TNNT2 | 191045 | Autosomal dominant |
| Xq28 Barth syndrome 302060 G4.5, TAZ 30039 X-linked | |||||
Abbreviations: ACTC1: actin, alpha, cardiac muscle; DTNA: dystrobrevin alpha; LVNC: left ventricular noncompaction MYBPC3: myosin-binding protein C, cardiac; MYH7: myosin heavy chain 7; TAZ ¼ tafazzin; TNNT2: troponin T2; TPM1: tropomyosin 1.