Genetic tests | Belgian Genetic Tests database

Full name	Analytes	Gene panels	Disease	Laboratory
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
MODY : Maturity onset Diabete of the Young (gene panel)	ABCC8, GCK, HNF1A, HNF4A, HNF1B, INS, KCNJ11	MODY - Maturity onset Diabete of the Young (21 genes) - IPG	MODY	Centre de Génétique-Institut de Pathologie et de Génétique (IPG)
Agammaglobulinemia	PIK3R1		Autosomal agammaglobulinemia	Centrum Menselijke Erfelijkheid - KUL
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
Cerebral cavernous malformation (gene panel)	KRIT1, CCM2, PDCD10	Cerebral cavernous malformation (3 genes) - UCL, Vascular malformations (germline) (38 genes) - UCL	Familial cerebral cavernous malformation	Centre de Génétique Médicale UCL

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