CSTB

cystatin B
OMIM: 601145, Gene2Phenotype

14 panels

Panel Reviews Mode of inheritance Details
14 panels

Amber CSTB in Epidermolysis bullosa


Level 2: Dermatological disorders
Version 1.15

review MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Sources
  • Expert Review Amber
  • Literature
Phenotypes
  • Keratolytic winter erythema (MIM#148370)
Tags
  • SV/CNV

Green CSTB in Mendeliome


Version 1.1891

review BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Victorian Clinical Genetics Services
Phenotypes
  • Epilepsy, progressive myoclonic 1A (Unverricht and Lundborg) MIM# 254800
  • Keratolytic winter erythema (MIM#148370)

Green CSTB in Genetic Epilepsy


Level 2: Neurology and neurodevelopmental disorders
Version 1.33

Component of the following Super Panels:

  • Progressive Neurological Conditions
  • review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • Victorian Clinical Genetics Services
    • Australian Genomics Health Alliance Epilepsy Flagship
    Phenotypes
    • Epilepsy, progressive myoclonic 1A (Unverricht and Lundborg) MIM# 254800
    Tags
    • 5'UTR
    • STR

    Green CSTB in Regression


    Level 2: Neurology and neurodevelopmental disorders
    Version 0.556

    review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • Expert Review
    Phenotypes
    • Epilepsy, progressive myoclonic 1A (Unverricht and Lundborg), MIM# 254800
    Tags
    • 5'UTR
    • STR

    Red CSTB in Intellectual disability syndromic and non-syndromic


    Level 2: Neurology and neurodevelopmental disorders
    Version 0.6063

    review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Red
    • Genetic Health Queensland
    Phenotypes
    • Epilepsy, progressive myoclonic 1A (Unverricht and Lundborg), MIM# 254800

    Green CSTB in Ataxia - paediatric


    Level 2: Neurology and neurodevelopmental disorders
    Version 1.26

    Component of the following Super Panels:

  • Ataxia_Superpanel
  • Neuromuscular Superpanel
  • Progressive Neurological Conditions
  • review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • Royal Melbourne Hospital
    Phenotypes
    • Epilepsy, progressive myoclonic 1A (Unverricht and Lundborg), MIM#254800
    Tags
    • 5'UTR
    • STR

    Green CSTB in Progressive Myoclonic Epilepsy


    Level 2: Neurology and neurodevelopmental disorders
    Version 0.19

    review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • Royal Melbourne Hospital
    Phenotypes
    • Epilepsy, progressive myoclonic 1A (Unverricht and Lundborg), MIM# 254800
    Tags
    • 5'UTR
    • STR

    Green CSTB 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
    • Epilepsy, progressive myoclonic 1A (Unverricht and Lundborg), 254800 (3)
    Tags
    • 5'UTR
    • STR

    Green CSTB in Additional findings_Paediatric


    Level 2: Screening
    Version 0.278

    review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • BabySeq Category A gene
    • Expert Review Green
    Phenotypes
    • Epilepsy, progressive myoclonic 1A

    Red CSTB in Fetal anomalies


    Version 1.255

    review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Red
    • Genomics England PanelApp
    • Genetic Health Queensland
    Phenotypes
    • Epilepsy, progressive myoclonic 1A (Unverricht and Lundborg), MIM# 254800

    Green CSTB in Prepair 1000+


    Level 2: Screening
    Version 1.9

    review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • Mackenzie's Mission
    Phenotypes
    • Epilepsy, progressive myoclonic 1A (Unverricht and Lundborg), 254800 (3)

    Red CSTB in BabyScreen+ newborn screening


    Level 2: Screening
    Version 1.113

    review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Red
    • BabySeq Category A gene
    Phenotypes
    • Epilepsy, progressive myoclonic 1A (Unverricht and Lundborg), MIM# 254800

    Green EPM1 STR in Ataxia - adult onset


    Level 2: Neurology and neurodevelopmental disorders
    Version 1.16

    Component of the following Super Panels:

  • Ataxia_Superpanel
  • Neurodegenerative disease - adult onset
  • Neuromuscular Superpanel
  • Progressive Neurological Conditions
  • review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • Literature
    Phenotypes
    • Epilepsy, progressive myoclonic 1A (Unverricht and Lundborg) MIM#254800
    Tags
    • STR

    Green EPM1 STR in Repeat Disorders


    Version 0.167

    review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • Expert list
    Phenotypes
    • Epilepsy, progressive myoclonic 1A (Unverricht and Lundborg) MIM#254800
    Tags
    • paediatric-onset