ZFYVE27

zinc finger FYVE-type containing 27
OMIM: 610243, Gene2Phenotype

6 panels

Panel	Reviews	Mode of inheritance	Details
Filter panels 6 panels
Red ZFYVE27 in Hereditary spastic paraplegia Level 3: Motor Disorders of the CNS Level 2: Neurology and neurodevelopmental disorders Version 1.316	review	MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown	Sources Expert Review Red Radboud University Medical Center, Nijmegen Expert list Illumina TruGenome Clinical Sequencing Services Phenotypes Spastic paraplegia 33, autosomal dominant
Red ZFYVE27 in Childhood onset hereditary spastic paraplegia Level 2: Neurology Version 9.1 Latest signed off version: v9.0 (6 May 2026)	review	MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown	Sources NHS GMS Yorkshire and North East GLH Illumina TruGenome Clinical Sequencing Services Expert Review Red Expert list Radboud University Medical Center, Nijmegen Phenotypes Spastic paraplegia 33, autosomal dominant
Red ZFYVE27 in Adult onset hereditary spastic paraplegia Level 2: Neurology Version 6.11 Latest signed off version: v6.10 (6 May 2026) Component of the following Super Panels: Adult-onset neurological disorders	review	MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown	Sources NHS GMS Yorkshire and North East GLH South West GLH Phenotypes Spastic paraplegia 33, autosomal dominant
Red ZFYVE27 in Adult onset neurodegenerative disorder Level 2: Neurology Version 9.1 Latest signed off version: v9.0 (6 May 2026) Component of the following Super Panels: Adult-onset neurological disorders	review	MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown	Sources Expert Review Red Phenotypes Spastic paraplegia 33, autosomal dominant
Red ZFYVE27 in Hereditary neuropathy Level 3: Motor and Sensory Disorders of the PNS Level 2: Neurology and neurodevelopmental disorders Version 1.508	review	Not set	Sources NHS GMS South West GLH Emory Genetics Laboratory Phenotypes Hereditary Neuropathies
Red ZFYVE27 in Hereditary neuropathy or pain disorder Level 2: Neurology Version 8.1 Latest signed off version: v8.0 (6 May 2026)	review	Not set	Sources NHS GMS South West GLH Emory Genetics Laboratory NHS GMS South West GLH Phenotypes Hereditary Neuropathies