Genetic tests | Belgian Genetic Tests database

Full name	Analytes	Gene panels	Disease	Laboratory
Rett syndrome / MECP2 Duplication Syndrome	MECP2		Rett syndrome	Centrum Menselijke Erfelijkheid - KUL
Rett syndrome	MECP2		Rett syndrome, Atypical Rett syndrome	Centre de Génétique Humaine - CHU Sart-Tilman
Hereditary Melanoma Panel (7 genes)	CDKN2A, CDK4, POT1, TERT, TERF2IP, BAP1, MITF	Hereditary Melanoma Panel (7 genes) - ULG	Familial melanoma	Centre de Génétique Humaine - CHU Sart-Tilman
Malignant Mesothelioma (BAP1; CDKN2A genes)	BAP1, CDKN2A			Centrum Menselijke Erfelijkheid - KUL
Melanoma (6 genes)	BAP1, CDK4, CDKN2A, MC1R, MITF, POT1	Melanoma (6 genes) - UCL	Familial melanoma, MITF-related melanoma and renal cell carcinoma predisposition syndrome, Uveal melanoma, Melanoma of soft tissue	Centre de Génétique Médicale UCL
Neuroblastoma (2 genes)	ALK, PHOX2B	Neuroblastoma (2 genes) - UCL	Neuroblastoma	Centre de Génétique Médicale UCL
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
Hypophosphatasia	ALPL		Adult hypophosphatasia, Infantile hypophosphatasia, Odontohypophosphatasia, Perinatal lethal hypophosphatasia, Childhood-onset hypophosphatasia, Prenatal benign hypophosphatasia	Centre de Génétique-Institut de Pathologie et de Génétique (IPG)

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