Han et al., 2020
- Thyroid hormone receptor α mutations cause heart defects in zebrafish.
Thyroid : official journal of the American Thyroid Association
31(2):315-326
Full text @ Thyroid
Marker Type | Symbol | Name |
---|---|---|
Gene | actn2b | actinin, alpha 2b |
Gene | atp2a2a | ATPase sarcoplasmic/endoplasmic reticulum Ca2+ transporting 2a |
Gene | hbae1.1 | hemoglobin, alpha embryonic 1.1 |
Gene | ldb3a | LIM domain binding 3a |
Gene | mybpc3 | myosin binding protein C3 |
Gene | myh6 | myosin, heavy chain 6, cardiac muscle, alpha |
Gene | myh7 | myosin heavy chain 7 |
Gene | mypn | myopalladin |
Gene | nexn | nexilin (F actin binding protein) |
Gene | pln1 | phospholamban 1 |
Gene | ryr2b | ryanodine receptor 2b (cardiac) |
Gene | slc8a1a | solute carrier family 8 member 1a |
Gene | smyd1b | SET and MYND domain containing 1b |
Gene | tcap | titin-cap (telethonin) |
Gene | thraa | thyroid hormone receptor alpha a |
Gene | thrab | thyroid hormone receptor alpha b |
Gene | thrb | thyroid hormone receptor beta |
Gene | tnnt2a | troponin T type 2a (cardiac) |