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Achromatopsia
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Alagille syndrome
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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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Prepair 1000+
Prepair 500+
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Short QT syndrome
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Speech apraxia
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Tubulinopathies
Usher Syndrome
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Vascular Malformations SuperPanel
Vitamin metabolism disorders
Vitreoretinopathy
Wilms Tumour
Version
Panel Version
2.0
1.40
Gene or Genomic Entity Name
MRTFB
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07 Jun 2026
Speech apraxia v2.0
MRTFB
Gene symbol changed from MKL2 to MRTFB during gene set migration (ENSG00000186260 -> ENSG00000186260)