Genetic tests | Belgian Genetic Tests database

Full name	Analytes	Gene panels	Disease	Laboratory
Leber hereditary optic neuropathy (LHON) (hot spot mutations - p.Ala53Thr in MT-ND1; p.Arg340His in MT-ND4; p.Met64Val in MT-ND6)	MT-ND1, MT-ND4, MT-ND6		Leber hereditary optic neuropathy	Centre de Génétique-Institut de Pathologie et de Génétique (IPG)
Leber hereditary optic neuropathy (LHON) (hot spot mutations - p.Ala53Thr in MT-ND1; p.Arg340His in MT-ND4; p.Met64Val in MT-ND6)	MT-ND1, MT-ND4, MT-ND6	LHON (3 genes) - VUB	Leber hereditary optic neuropathy	Centrum Medische Genetica - UZ Brussel VUB
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
Kabuki syndrome (gene panel)	KMT2D, KDM6A, KMT2A, HNRNPK, RAP1A, RAP1B, PACS1	Kabuki (7 genes) - IPG	Kabuki syndrome	Centre de Génétique-Institut de Pathologie et de Génétique (IPG)
Maternally-inherited diabetes and deafness / Mitochondrial myopathy with reversible cytochrome C oxidase deficiency / mitochondrial tRNA glutamic acid	MT-TE		Maternally-inherited diabetes and deafness, MELAS	Centrum Medische Genetica - UZ Brussel VUB

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