Burkhalter et al., 2019 - Imbalanced mitochondrial function provokes heterotaxy via aberrant ciliogenesis. The Journal of Clinical Investigation   130:2841-2855 Full text @ Journal of Clin. Invest.
26 Genes / Markers
Marker Type Symbol Name
Gene acox1 acyl-CoA oxidase 1, palmitoyl
Gene akap1b A kinase (PRKA) anchor protein 1b
Gene alas2 aminolevulinate, delta-, synthase 2
Gene apex2 APEX nuclease (apurinic/apyrimidinic endonuclease) 2
Gene ca5a carbonic anhydrase Va
Gene chchd3a coiled-coil-helix-coiled-coil-helix domain containing 3a
Gene coq8b coenzyme Q8B
Gene coq9 coenzyme Q9 homolog (S. cerevisiae)
Gene cox5aa cytochrome c oxidase subunit 5Aa
Gene dand5 DAN domain family, member 5
Gene gapdh glyceraldehyde-3-phosphate dehydrogenase
Gene idh3g isocitrate dehydrogenase (NAD(+)) 3 non-catalytic subunit gamma
Gene ins preproinsulin
Gene mrpl38 mitochondrial ribosomal protein L38
Gene mrpl44 mitochondrial ribosomal protein L44
Gene mrps25 mitochondrial ribosomal protein S25
Gene mtrr 5-methyltetrahydrofolate-homocysteine methyltransferase reductase
Gene myl7 myosin, light chain 7, regulatory
Gene ndufa1 NADH:ubiquinone oxidoreductase subunit A1
Gene osbpl1a oxysterol binding protein-like 1A
Gene phka1b phosphorylase kinase, alpha 1b (muscle)
Gene phka2 phosphorylase kinase, alpha 2 (liver)
Gene slc25a5 solute carrier family 25 member 5
Gene spaw southpaw
Gene tafazzin tafazzin, phospholipid-lysophospholipid transacylase
Gene timm17b translocase of inner mitochondrial membrane 17 homolog B (yeast)