Table 3 Genes associated with heterotaxy in humans

Autosomal dominant

ACVR2B, CFC1, CRELD1, FOXH1, LEFTY1, LEFTY2, NKX2.5, NODAL

Autosomal recessive

CFAP53, GDF1, MMP21, MNS1, PKD1L1

Autosomal recessive (Primary ciliary dyskinesia)

ARMC4, CCDC103, CCDC114, CCDC151, CCDC39, CCDC40, CCDC65, CCNO, CFAP298, CFAP300, DNAAF1, DNAAF2, DNAAF3, DNAAF4, DNAAF5, DNAH1, DNAH11, DNAH5, DNAH9, DNAI1, DNAI2, DNAJB13, DNAL1, DRC1, FOXJ1, GAS2L2, GAS8, HYDIN, LRRC56, LRRC6, MCIDAS

NEK10, NME8, PIH1D3, RSPH1, RSPH3, RSPH4A, RSPH9, SPAG1, STK36, TP73, TTC12, TTC25, ZMYND10

X-Linked

ZIC3