ARL6IP1

ADP ribosylation factor like GTPase 6 interacting protein 1
OMIM: 607669, Gene2Phenotype

7 panels

Panel	Reviews	Mode of inheritance	Details
Filter panels 7 panels
Red ARL6IP1 in Hereditary spastic paraplegia Level 3: Motor Disorders of the CNS Level 2: Neurology and neurodevelopmental disorders Version 1.316	review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Red Expert list
Green ARL6IP1 in Childhood onset hereditary spastic paraplegia Level 2: Neurology Version 8.30 Latest signed off version: v8.0 (30 Apr 2025)	review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green NHS GMS Yorkshire and North East GLH Expert list Phenotypes Spastic paraplegia 61, autosomal recessive, OMIM:615685 hereditary spastic paraplegia 61, MONDO:0014304
Amber ARL6IP1 in Adult onset hereditary spastic paraplegia Level 2: Neurology Version 6.7 Latest signed off version: v6.0 (30 Apr 2025)	review	BIALLELIC, autosomal or pseudoautosomal	Sources London North GLH Expert Review Amber NHS GMS Yorkshire and North East GLH South West GLH Phenotypes Spastic paraplegia 61, autosomal recessive, 615685
Red ARL6IP1 in Adult onset neurodegenerative disorder Level 2: Neurology Version 8.11 Latest signed off version: v8.0 (30 Apr 2025)	review	BIALLELIC, autosomal or pseudoautosomal	Sources Yorkshire and North East GLH NHS GMS South West GLH Expert Review Red
Green ARL6IP1 in Fetal anomalies Level 2: Fetal (including NIPD) Version 6.140 Latest signed off version: v6.0 (30 Apr 2025)	review	BIALLELIC, autosomal or pseudoautosomal	Sources NHS GMS Expert Review Green Phenotypes Spastic paraplegia 61, autosomal recessive, OMIM:615685
Red ARL6IP1 in Hereditary neuropathy Level 3: Motor and Sensory Disorders of the PNS Level 2: Neurology and neurodevelopmental disorders Version 1.506	review	BIALLELIC, autosomal or pseudoautosomal	Sources NHS GMS London North GLH Phenotypes Spastic paraplegia 61, autosomal recessive, 615685 Childhood onset spastic paraplegia with mutilating, sensory to motor axonal neuropathy
Green ARL6IP1 in Hereditary neuropathy or pain disorder Level 2: Neurology Version 7.36 Latest signed off version: v7.0 (30 Apr 2025)	review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green London North GLH NHS GMS NHS GMS London North GLH Phenotypes Spastic paraplegia 61, autosomal recessive, 615685 Childhood onset spastic paraplegia with mutilating, sensory to motor axonal neuropathy