Genomics England

ZFYVE26

zinc finger FYVE-type containing 26

OMIM: 612012

Panel	Mode of inheritance	Details
Filter panels8 panels
Green in Adult onset hereditary spastic paraplegia R-numbers: R60 Signed-off version 3.14	BIALLELIC, autosomal or pseudoautosomal	Phenotypes Spastic paraplegia 15, autosomal recessive, 270700
Green in Adult onset leukodystrophy R-numbers: R62 Signed-off version 3.0	BIALLELIC, autosomal or pseudoautosomal	Phenotypes Spastic paraplegia 15, autosomal recessive, 270700
Green in Childhood onset hereditary spastic paraplegia R-numbers: R61 Signed-off version 4.0	BIALLELIC, autosomal or pseudoautosomal	Phenotypes Spastic paraplegia 15, autosomal recessive, 270700
Green in DDG2P Component of the following Super Panels: - Paediatric disorders Signed-off version 3.1	BIALLELIC, autosomal or pseudoautosomal	Phenotypes SPASTIC PARAPLEGIA AUTOSOMAL RECESSIVE TYPE 15 270700
Green in Hereditary ataxia with onset in adulthood R-numbers: R54 Signed-off version 4.0	BIALLELIC, autosomal or pseudoautosomal	Phenotypes Autosomal recessive spastic paraplegia 15, 270700, Autosomal recessive spastic paraplegia 15, 270700
Green in Intellectual disability - microarray and sequencing Component of the following Super Panels: - Childhood onset leukodystrophy - Hypotonic infant - Paediatric disorders R-numbers: R29 Signed-off version 5.0	BIALLELIC, autosomal or pseudoautosomal	Phenotypes SPASTIC PARAPLEGIA AUTOSOMAL RECESSIVE TYPE 15 (SPG15)
Green in Retinal disorders R-numbers: R32 Signed-off version 4.0	BIALLELIC, autosomal or pseudoautosomal	Phenotypes Spastic paraplegia 15, autosomal recessive OMIM:270700
Green in White matter disorders and cerebral calcification - narrow panel Component of the following Super Panels: - Childhood onset leukodystrophy Signed-off version 3.0	BIALLELIC, autosomal or pseudoautosomal	Phenotypes Spastic paraplegia 15, autosomal recessive, OMIM:270700