Genetic tests | Belgian Genetic Tests database

Full name	Analytes	Gene panels	Disease	Laboratory
Oculopharyngeal Muscular Dystrophy - GCN repeats expansion	PABPN1		Oculopharyngeal muscular dystrophy	Centrum Menselijke Erfelijkheid - KUL
Oculopharyngeal muscular dystrophy - PABPN1 gene GCN trinucleotide repeats	PABPN1		Oculopharyngeal muscular dystrophy	Centrum Medische Genetica - UZ Brussel VUB
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)
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
Susceptibility to Cutaneous Malignant Melanoma	CDK4		Familial melanoma	Centre de Génétique Humaine - CHU Sart-Tilman
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
Canavan disease (hot spot mutation - p.Glu285Ala, p.Tyr231*)	ASPA		Mild Canavan disease, Severe Canavan disease	Centrum Medische Genetica - UZ Antwerpen
Jewish mutation panel (Tay Sachs, Fanconi, Dysautonomia, Canavan) (4 genes; 7 hot spot mutations)	ASPA, ELP1, HEXA, FANCC	Hot spot mutation among Jewish (4 genes, 7 mutations) - UZA		Centrum Medische Genetica - UZ Antwerpen

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