SLC41A1

solute carrier family 41 member 1
OMIM: 610801, Gene2Phenotype

5 panels

Panel Reviews Mode of inheritance Details
5 panels

Red SLC41A1 in Parkinson Disease and Complex Parkinsonism

Level 3: Neurodegenerative disorders
Level 2: Neurology and neurodevelopmental disorders
Version 1.68

review Not set
Sources
  • Expert Review Red
  • Radboud University Medical Center, Nijmegen
Phenotypes
  • Parkinson disease (Yan (2011) Int J Neurosci 121,632)

Red SLC41A1 in Ductal plate malformation


Version 1.11

review Unknown
Sources
  • Expert list
Phenotypes
  • No OMIM

Red SLC41A1 in Neurodegenerative disorders - adult onset


Version 2.33
Signed off v.2.31 on 8 Oct 2020

review Unknown
Sources
  • Expert Review Red
Phenotypes
  • Parkinson disease (Yan (2011) Int J Neurosci 121,632)

Red SLC41A1 in Adult onset movement disorder


Version 1.16
Signed off v.1.14 on 15 Oct 2020

review Not set
Sources
  • NHS GMS
  • South West GLH
  • Expert Review Red
Phenotypes
  • Parkinson disease (Yan (2011) Int J Neurosci 121,632)

Red SLC41A1 in Renal ciliopathies

Level 3: Congenital malformations caused by ciliopathies
Level 2: Ciliopathies
Version 1.31
Signed off v.1.2 on 4 Mar 2020

Component of the following Super Panels:

  • Cystic renal disease
  • Paediatric disorders
  • Rare multisystem ciliopathy Super panel
  • Renal superpanel - broad
  • Renal superpanel - narrow
  • review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Red
    • Expert list
    Phenotypes
    • Nephronophthisis