Genetic tests | Belgian Genetic Tests database

Full name	Analytes	Gene panels	Disease	Laboratory
Cardiofaciocutaneous syndrome (5 genes)	HRAS, KRAS, BRAF, MAP2K2, MAP2K1		Cardiofaciocutaneous syndrome	Centre de Génétique Humaine - CHU Sart-Tilman
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
Hypermethylation promoter MLH1 and p.V600 of BRAF1	MLH1, BRAF		Lynch syndrome	Centrum Menselijke Erfelijkheid - KUL
Lynch syndrome - MLH1 promoter hypermethylation and BRAF V600E mutation	MLH1, BRAF		Selection of therapeutic option in colorectal cancer	Centre de Génétique Humaine - CHU Sart-Tilman
Obesity (gene panel)	ADCY3, BDNF, LEP, LEPR, MC3R, MC4R, NR0B2, NTRK2, PCSK1, POMC, SIM1, UCP3	Obesitas (genepanel) - UZA		Centrum Medische Genetica - UZ Antwerpen
Obesitas, early onset (gene panel)	MC4R, MC3R, LEP, LEPR, PCSK1, POMC, SIM1, NTRK2	Obesitas, early onset (8 genes) - VUB		Centrum Medische Genetica - UZ Brussel VUB
Spinocerebellar ataxia (SCA) types 8, 10, 12, 17 - repeat expansion	ATXN8, ATXN10, PPP2R2B, TBP	Spinocerebellar ataxia (type 8, 10, 12, 17) (4 genes) - UZA	Spinocerebellar ataxia type 8, Spinocerebellar ataxia type 10, Spinocerebellar ataxia type 12, Spinocerebellar ataxia type 17	Centrum Medische Genetica - UZ Antwerpen

Did not find what you were looking for? Contact us through the support center.