SACS

sacsin molecular chaperone
OMIM: 604490, Gene2Phenotype

18 panels

Panel Reviews Mode of inheritance Details
18 panels

Green SACS in Cerebral Palsy


Level 2: Neurology and neurodevelopmental disorders
Version 1.389

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Literature
Phenotypes
  • Spastic ataxia, Charlevoix-Saguenay type MIM#270550
Tags
  • SV/CNV

Green SACS in Mendeliome


Version 1.2512

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Expert list
  • Victorian Clinical Genetics Services
Phenotypes
  • Spastic ataxia, Charlevoix-Saguenay type MIM#270550
Tags
  • SV/CNV

Amber SACS in Genetic Epilepsy


Level 2: Neurology and neurodevelopmental disorders
Version 1.145

Component of the following Super Panels:

  • Progressive Neurological Conditions
  • review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Amber
    • Literature
    Phenotypes
    • Spastic ataxia, Charlevoix-Saguenay type MIM#270550

    Green SACS in Mitochondrial disease


    Level 2: Metabolic disorders
    Version 0.973

    Component of the following Super Panels:

  • Metabolic Disorders Superpanel
  • Progressive Neurological Conditions
  • review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert list
    • Expert Review Green
    • Expert list
    Phenotypes
    • Spastic ataxia, Charlevoix-Saguenay type, MIM# 270550

    Green SACS in Regression


    Level 2: Neurology and neurodevelopmental disorders
    Version 0.577

    review Unknown
    Sources
    • Victorian Clinical Genetics Services
    • Expert Review Green

    Amber SACS in Intellectual disability syndromic and non-syndromic


    Level 2: Neurology and neurodevelopmental disorders
    Version 1.118

    review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Amber
    • Genetic Health Queensland
    Phenotypes
    • Spastic ataxia, Charlevoix-Saguenay type, MIM# 270550

    Green SACS in Ataxia - adult onset


    Level 2: Neurology and neurodevelopmental disorders
    Version 1.46

    Component of the following Super Panels:

  • Ataxia_Superpanel
  • Neurodegenerative disease - adult onset
  • Neuromuscular Superpanel
  • Progressive Neurological Conditions
  • review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert list
    • Royal Melbourne Hospital
    • Expert Review Green
    Phenotypes
    • Spastic ataxia, Charlevoix-Saguenay type
    • Charlevoix-Saguenay spastic ataxia, 270550

    Green SACS in Ataxia - paediatric


    Level 2: Neurology and neurodevelopmental disorders
    Version 1.34

    Component of the following Super Panels:

  • Ataxia_Superpanel
  • Neuromuscular Superpanel
  • Progressive Neurological Conditions
  • review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • Expert list
    Phenotypes
    • Spastic ataxia, Charlevoix-Saguenay type MIM#270550

    Green SACS in Hereditary Spastic Paraplegia - adult onset


    Level 2: Neurology and neurodevelopmental disorders
    Version 1.13

    Component of the following Super Panels:

  • Hereditary Spastic Paraplegia Superpanel
  • Neurodegenerative disease - adult onset
  • Neuromuscular Superpanel
  • Progressive Neurological Conditions
  • review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • Expert list
    • Royal Melbourne Hospital
    Phenotypes
    • Spastic ataxia, Charlevoix-Saguenay type, 270550
    • MONDO:0010041
    Tags
    • SV/CNV

    Green SACS in Hereditary Spastic Paraplegia - paediatric


    Level 2: Neurology and neurodevelopmental disorders
    Version 1.90

    Component of the following Super Panels:

  • Hereditary Spastic Paraplegia Superpanel
  • Neuromuscular Superpanel
  • Progressive Neurological Conditions
  • review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • Expert list
    Phenotypes
    • Spastic ataxia, Charlevoix-Saguenay type, MIM@ 270550

    Green SACS in Hereditary Neuropathy - complex


    Level 2: Neurology and neurodevelopmental disorders
    Version 1.27

    Component of the following Super Panels:

  • Hereditary Neuropathy_CMT_IsolatedAndComplex
  • Neuromuscular Superpanel
  • Progressive Neurological Conditions
  • review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • Royal Melbourne Hospital
    Phenotypes
    • Charlevoix-Saguenay spastic ataxia (MONDO:0010041
    • MIM#270550)
    Tags
    • SV/CNV

    Green SACS in Mackenzie's Mission_Reproductive Carrier Screening


    Level 2: Screening
    Version 0.109

    review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • Mackenzie's Mission
    Phenotypes
    • Spastic ataxia, Charlevoix-Saguenay type, 270550 (3)

    Green SACS in Additional findings_Paediatric


    Level 2: Screening
    Version 0.278

    review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • BabySeq Category A gene
    • Expert Review Green
    Phenotypes
    • Spastic ataxia Charlevoix-Saguenay type

    Green SACS in Congenital nystagmus


    Level 2: Ophthalmological disorders
    Version 1.22

    review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • Genomics England PanelApp
    • NHS Genomic Medicine Service
    • Expert Review Green
    • Expert list
    Phenotypes
    • Spastic ataxia, Charlevoix-Saguenay type, MIM# 270550

    Red SACS in Fetal anomalies


    Version 1.321

    review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Red
    • Genomics England PanelApp
    • Genetic Health Queensland
    Phenotypes
    • Spastic ataxia, Charlevoix-Saguenay type, MIM# 270550

    Green SACS in Prepair 1000+


    Level 2: Screening
    Version 2.7

    review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • Mackenzie's Mission
    Phenotypes
    • Spastic ataxia, Charlevoix-Saguenay type, MIM#270550
    Tags
    • SV/CNV

    Red SACS in Genomic newborn screening: BabyScreen+


    Level 2: Screening
    Version 1.117

    review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Red
    • BabySeq Category A gene
    Phenotypes
    • Spastic ataxia, Charlevoix-Saguenay type MIM#270550

    Green SACS in Prepair 500+


    Level 2: Screening
    Version 1.165

    review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • Expert Review Green
    • Mackenzie's Mission
    • Mackenzie's Mission
    Phenotypes
    • Spastic ataxia, Charlevoix-Saguenay type, 270550 (3)