Genetic tests | Belgian Genetic Tests database

Full name	Analytes	Gene panels	Disease	Laboratory
Mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes (MELAS) (hot spot mutation - m.3243A>G)	MT-TL1		MELAS	Centre de Génétique-Institut de Pathologie et de Génétique (IPG)
Diabetes, mitochondrial (hot spot mutation - m.3243A>G, MTTL1 (tRNA-Leu) )	MT-TL1		MELAS	Centrum Medische Genetica - UZ Antwerpen
Mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes (MELAS) (full sequencing)	MT-TL1		MELAS	Centrum Medische Genetica - UZ Brussel VUB
Mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes (MELAS) (hot spot mutation - m.3243A>G)	MT-TL1		MELAS	Centrum Medische Genetica - UZ Brussel VUB
Vascular malformations (somatic)	AKT1, AKT2, AKT3, ALK, BRAF, GNA11, GNA14, GNAQ, HRAS, IDH1, IDH2, KRAS, NRAS, PIK3CA, PIK3R1, PIK3R2, PTEN, TEK, MAP3K3, MAP2K1	Vascular malformations (somatic) (19 genes) - UCL	Capillary malformation-arteriovenous malformation, CLOVES syndrome, Maffucci syndrome, Proteus syndrome	Centre de Génétique Médicale UCL
Perrault syndrome (gene panel)	TWNK, CLPP, HARS2, HSD17B4, LARS2	Perrault syndrome (5 genes) - UZA	Perrault syndrome	Centrum Medische Genetica - UZ Antwerpen
Alport autosomal recessive and X-linked and hematuria (3 genes)	COL4A3, COL4A4, COL4A5	Alport (X-linked and recessive) (3 genes) - IPG	Autosomal recessive Alport syndrome, X-linked Alport syndrome	Centre de Génétique-Institut de Pathologie et de Génétique (IPG)

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