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Achromatopsia
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IBMDx study
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Kidneyome_SuperPanel
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Liverome Superpanel
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Myopathy Superpanel
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Pierre Robin Sequence
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Prepair 1000+
Prepair 500+
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Renal Cystic Disease_SuperPanel
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Retinal Disorders Superpanel
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Thyroid Cancer
Transplant Co-Morbidity
Tuberous Sclerosis_Focal Cortical Dysplasia_Hemimegalencephaly
Tubulinopathies
Usher Syndrome
Vascular Malformations_Germline
Vascular Malformations_Somatic
Vascular Malformations SuperPanel
Vitamin metabolism disorders
Vitreoretinopathy
Wilms Tumour
Version
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2.0
1.25
Gene or Genomic Entity Name
ATP5MC3
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07 Jun 2026
Mitochondrial disease v2.0
ATP5MC3
Gene symbol changed from ATP5G3 to ATP5MC3 during gene set migration (ENSG00000154518 -> ENSG00000154518)