TABLE 1.
Gene symbol | Gene name | First/second‐order cilia gene | Mutant phenotype | Reference |
---|---|---|---|---|
ARMC4 | Armadillo repeat containing 4 | First order | Laterality defects, cardiac looping defects | (Hjeij et al., 2013; Onoufriadis et al., 2014) |
CCDC 40 | Coiled‐coil domain containing 40 | First order | Laterality defects, cardiac looping defects | (Becker‐Heck et al., 2011; Sugrue & Zohn, 2017) |
CCDC151 | Coiled‐coil domain containing 151 | First order | Laterality defects, dextrocardia, ventricular septal defects | (Hjeij et al., 2014) |
CCDC39 | Coiled‐coil domain containing 39 | First order | Laterality defects, cardiac looping defects | (Solomon et al., 2017) |
CRELD1 | Cysteine Rich With EGF Like Domains 1 | Second order | Atrioventricular septal defects (AVSDs), valve defects | (Beckert et al., 2021, Burnicka‐Turek et al., 2016) |
DHH | Desert hedgehog | Second order | Mitral valve prolapse (MVP) | (Fulmer et al., 2020) |
DNAAF1 | Dynein axonemal assembly factor 1 | First order | Laterality defects, cardiac looping defects | (Hartill et al., 2018) |
DNAAF3 | Dynein axonemal assembly factor 3 | First order | Laterality defects, cardiac looping defects | (Mitchison et al., 2012) |
DNAH5 | Dynein axonemal heavy chain 5 | First order | Laterality defects, cardiac looping defects | (Nöthe‐Menchen et al., 2019) |
DNAH6 | Dynein axonemal heavy chain 6 | First order | Laterality defects, cardiac looping defects | (Y. Li et al., 2016) |
DNAH7 | Dynein axonemal heavy chain 7 | First order | Laterality defects, cardiac looping defects | (Y. J. Zhang et al., 2002) |
DNAH 10 | Dynein axonemal heavy chain 10 | First order | Laterality defects, cardiac looping defects | (C. Liu et al., 2018) |
DNAH11 | Dynein axonemal heavy chain 11 | First order | Laterality defects, AVSDs | (Bartoloni et al., 2002; Burnicka‐Turek et al., 2016; Dougherty et al., 2016; S. Liu et al., 2019; Xia et al., 2021) |
DNAIC1 | Dynein Axonemal Intermediate Chain 1 | First order | Laterality defects, cardiac looping defects | (Francis et al., 2012) |
DYX1C1(DNAAF4) | Dyslexia Susceptibility 1 Candidate 1 | First order | Laterality defects, cardiac looping defects | (Tarkar et al., 2013) |
DZIP1 | DAZ interacting zinc finger protein 1 | First order | MVP | (Toomer et al., 2019) |
EXOC5 | Exocyst complex component 5 | First order | Bicuspid aortic valve disease and aortic stenosis | (Fulmer et al., 2019) |
FTM (Rpgrip1l) | Fantom | First order | Laterality defects, cardiac looping defects, AVSD | (Gerhardt et al., 2013; Vierkotten et al., 2007) |
GPR22 | G protein‐coupled receptor (GPCR) 22 | First order | Laterality defects, cardiac looping defects, cardiac edema | (Verleyen et al., 2014) |
GRK5 | GPCR kinase 5 | Second order | Laterality defects, cardiac looping defects, valve development defects | (Burkhalter et al., 2013; Casar Tena et al., 2015) |
IFT20 | Intraflagellar transport 20 | First order | Proepicardial organ and myocardial tissue size defects | (Peralta et al., 2020) |
IFT46 | Intraflagellar transport 46 | First order | Laterality defects, cardiac looping defects | (Lee et al., 2015) |
IFT54 (TRAF3IP1) | Intraflagellar transport 54(TRAF3 interacting protein 1) | First order | Proepicardial organ and myocardial tissue size defects | (Peralta et al., 2020) |
IFT57 | Intraflagellar transport 57 | First order | Laterality defects, cardiac looping defects | (Houde et al., 2006) |
IFT74 | Intraflagellar transport 74 | First order | Laterality defects, cardiac looping defects, AVSD, hypoplastic left heart | (Bakey et al., 2023) |
IFT88 | Intraflagellar transport 88 | First order | Laterality defects, cardiac looping defects, outflow tract defects, ventricular trabeculation defects, cardiac cushion EMT defects, valves defects, proepicardial organ and myocardial tissue size defects | (Burns et al., 2019; Clement et al., 2009; Murcia et al., 2000; Peralta et al., 2020; Toomer et al., 2019; Willaredt et al., 2012) |
IFT172 | Intraflagellar transport 172 | First order | Laterality defects, cardiac looping defects | (Gorivodsky et al., 2009) |
INVS | Inversin | First order | Laterality defects, cardiac looping defects | (Lowe et al., 1996, Okada et al., 1999; Watanabe et al., 2003; Yokoyama et al., 1993) |
KIF3A | kinesin family member 3A | First order | Laterality defects, cardiac looping defects | (Takeda et al., 1999) |
KIF3B | kinesin family member 3B | First order | Laterality defects, cardiac looping defects | (Nonaka et al., 1998) |
MEGF8 | Multiple Epidermal Growth Factor‐like Domains 8 | Second order | Laterality defects, cardiac looping defects | (Y. Li et al., 2015; Z. Zhang et al., 2009) |
MKS1 | MKS Transition Zone Complex Subunit 1 | First order | AVSDs | (Burnicka‐Turek et al., 2016; Cui et al., 2011) |
MNS1 | Meiosis specific nuclear structural 1 | First order | Laterality defects | (Ta‐Shma et al., 2018) |
PDGFR‐α | Platelet‐derived growth factor receptor‐alpha | Second order | MVP | (Moore et al., 2021) |
PKD1 | Polycystin 1, transient receptor potential channel interacting | First order | AVSDs, myocardial wall thinning, double‐outlet right ventricle, cardiac valves defects | (Boulter et al., 2001; Juan et al., 2023) |
PKD1L1 | Polycystin 1 like 1, transient receptor potential channel interacting | First order | Laterality defects, cardiac looping defects, cardiac valve defects | (Field et al., 2011; Juan et al., 2023) |
PKD2 | Polycystin 2, transient receptor potential cation channel | First order | Laterality defects, cardiac looping defects, cardiac septation defects, cardiac valve defects | (Juan et al., 2023; Pennekamp et al., 2002; G. Wu et al., 2000) |
TBC1D32 | TBC1 domain family member 32 | First order | Laterality defects, cardiac looping defects | (Y. Li et al., 2015) |
TCTN2 | Tectonic family member 2 | First order | Ventricular septal defects | (Sang et al., 2011) |
TTC25 | Tetratricopeptide repeat domain 25 | First order | Laterality defects, cardiac looping defects | (Wallmeier et al., 2016) |
Note: First‐order genes are those that encode proteins required to form the cilia, cilia motility, or for cilia cargo transport. Second‐order genes are those that participate in signaling at the cilium or have undefined roles in the cilium.