Liu et al., 2018 - Rare copy number variants analysis identifies novel candidate genes in heterotaxy syndrome patients with congenital heart defects. Genome Medicine   10:40 Full text @ Genome Med.
10 Genes / Markers
Marker Type Symbol Name
Gene cfap46 cilia and flagella associated protein 46
Gene dnah10 dynein axonemal heavy chain 10
Gene galnt11 UDP-N-acetyl-alpha-D-galactosamine:polypeptide N-acetylgalactosaminyltransferase 11 (GalNAc-T11)
Gene lft2 lefty2
lincRNA Gene linc.cfap46 lincRNA gene cfap46
Gene numb NUMB endocytic adaptor protein
Gene pacrg PARK2 co-regulated
Gene pitx2 paired-like homeodomain 2
Gene rnf115a ring finger protein 115a
Gene tctn2 tectonic family member 2
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