ARL6IP1

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

6 panels

Panel Reviews Mode of inheritance Details
6 panels
Red ARL6IP1 in Hereditary spastic paraplegia

Level 3: Motor Disorders of the CNS
Level 2: Neurology and neurodevelopmental disorders
Version 1.311

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Red
  • Expert list
Green ARL6IP1 in Childhood onset hereditary spastic paraplegia


Version 4.43
Latest signed off version: v4.0 (22 Mar 2023)

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


Version 3.21
Latest signed off version: v3.14 (31 Jul 2023)

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


Version 4.47
Latest signed off version: v4.34 (31 Jul 2023)

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Yorkshire and North East GLH
  • NHS GMS
  • South West GLH
  • Expert Review Red
Red ARL6IP1 in Hereditary neuropathy

Level 3: Motor and Sensory Disorders of the PNS
Level 2: Neurology and neurodevelopmental disorders
Version 1.477

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
Red ARL6IP1 in Hereditary neuropathy or pain disorder


Version 3.94
Latest signed off version: v3.24 (15 May 2023)

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • 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