Genomics England

TRK-fused gene

Panel	Mode of inheritance	Details
Filter panels3 panels
Green in Childhood onset hereditary spastic paraplegia R-numbers: R61 Signed-off version 6.4	BIALLELIC, autosomal or pseudoautosomal	Phenotypes Spastic paraplegia 57, autosomal recessive, OMIM:615658
Green in Hereditary neuropathy or pain disorder R-numbers: R78 Signed-off version 5.16	BOTH monoallelic and biallelic, autosomal or pseudoautosomal	Phenotypes Hereditary motor and sensory neuropathy, Okinawa type, OMIM:604484, Spastic paraplegia 57, autosomal recessive, OMIM:615658
Green in Optic neuropathy R-numbers: R41 Signed-off version 4.0	BIALLELIC, autosomal or pseudoautosomal	Phenotypes Spastic paraplegia 57, autosomal recessive, OMIM:615658