Gene List:
ACVR2B, ARMC4, C21ORF59, CCDC103, CCDC114, CCDC151, CCDC39, CCDC40, CFAP53, DNAAF1, DNAAF2, DNAAF3, DNAAF5, DNAH11, DNAH5, DNAI1, DNAI2, DNAL1, DYX1C1, FOXH1, GDF1, INVS, LEFTY2, LRRC6, MMP21, NODAL, PIH1D3, PKD1L1, SPAG1, ZIC3, ZMYND10

References:
Zhang W, et al. Whole-exome sequencing identifies a novel CCDC151 mutation, c.325G>T (p.E109X), in a patient with primary ciliary dyskinesia and situs inversus. J Hum Genet 64, 249–252 (2019)

Cowan J, et al. Copy number variation as a genetic basis for heterotaxy and heterotaxy-spectrum congenital heart defects. Philos Trans R Soc Lond B Biol Sci. 2016 Dec 19;371(1710).

Robinson PJ, et al. Situs inversus: When an incidental finding is not so incidental. Paediatr Child Health. 2017 Jul;53(7):715-716.