SKIV2L

Ski2 like RNA helicase
OMIM: 600478, Gene2Phenotype

11 panels

Panel Reviews Mode of inheritance Details
11 panels
Green SKIV2L in Infantile enterocolitis & monogenic inflammatory bowel disease

Level 3: Gastrointestinal disorders
Level 2: Gastroenterological disorders
Version 1.45

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • UKGTN
  • Illumina TruGenome Clinical Sequencing Services
  • Radboud University Medical Center, Nijmegen
  • Expert list
Phenotypes
  • Trichohepatoenteric syndrome 2 614602
Tags
  • new-gene-name
Green SKIV2L in Gastrointestinal epithelial barrier disorders

Level 3: Gastrointestinal disorders
Level 2: Gastroenterological disorders
Version 1.76

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • UKGTN
  • Expert list
  • Illumina TruGenome Clinical Sequencing Services
  • Radboud University Medical Center, Nijmegen
Phenotypes
  • Trichohepatoenteric syndrome 2, 614602
  • Trichohepatoenteric Syndrome
  • Inflammatory Bowel Disease (Very Early Onset)
Tags
  • new-gene-name
Green SKIV2L in COVID-19 research


Level 2: Viral research
Version 1.146

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • London North GLH
  • GOSH PID v.8.0
  • NHS GMS
  • North West GLH
  • ESID Registry 20171117
  • Expert Review Green
  • NHS GMS
  • North West GLH
  • London North GLH
  • Expert Review Green
  • ESID Registry 20171117
  • GOSH PID v.8.0
Phenotypes
  • Trichohepatoenteric syndrome 2,614602
  • Immune dysfunction
  • Trichohepatoenteric syndrome
Tags
  • new-gene-name
Green SKIV2L in Intestinal failure or congenital diarrhoea


Level 2: Gastrohepatology
Version 3.7
Latest signed off version: v3.0 (22 Mar 2023)

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Other
  • NHS GMS
Phenotypes
  • Trichohepatoenteric syndrome 2, OMIM:614602
Tags
  • new-gene-name
Green SKIV2L in Primary immunodeficiency or monogenic inflammatory bowel disease


Level 2: Immunology
Version 8.78
Latest signed off version: v8.0 (30 Apr 2025)

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • NHS GMS
  • North West GLH
  • London North GLH
  • Expert Review Green
  • ESID Registry 20171117
  • GOSH PID v.8.0
Phenotypes
  • Trichohepatoenteric syndrome 2,614602
  • Trichohepatoenteric syndrome
  • Immune dysfunction
Tags
  • early-onset
  • new-gene-name
Green SKIV2L in Undiagnosed metabolic disorders

Level 3: Specific metabolic abnormalities
Level 2: Metabolic disorders
Version 1.642

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Literature
Phenotypes
  • Trichohepatoenteric syndrome 2 (Other metabolic disorders)
  • Infantile enterocolitis & monogenic inflammatory bowel disease
Tags
  • new-gene-name
Green SKIV2L in Likely inborn error of metabolism


Level 2: Metabolic
Version 8.91
Latest signed off version: v8.0 (30 Apr 2025)

Component of the following Super Panels:

  • Childhood onset leukodystrophy
  • Hypotonic infant
  • Paediatric disorders
  • Unexplained death in infancy and sudden unexplained death in childhood
  • review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • London North GLH
    • NHS GMS
    Phenotypes
    • Infantile enterocolitis & monogenic inflammatory bowel disease
    • Trichohepatoenteric syndrome 2 (Other metabolic disorders)
    Tags
    • new-gene-name
    Green SKIV2L 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
    • Expert Review Green
    • NHS GMS
    • PAGE DD-Gene2Phenotype
    Phenotypes
    • Trichohepatoenteric syndrome 2, OMIM:614602
    Tags
    • new-gene-name
    Green SKIV2L in DDG2P


    Version 6.424
    Latest signed off version: v6.0 (30 Apr 2025)

    Component of the following Super Panels:

  • Paediatric disorders
  • review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • DD-Gene2Phenotype
    • Expert Review Green
    Phenotypes
    • TRICHOHEPATOENTERIC SYNDROME 2 615602
    Tags
    • new-gene-name
    Red SKIV2L in Intellectual disability


    Level 2: Developmental disorders
    Version 9.285
    Latest signed off version: v9.0 (30 Apr 2025)

    Component of the following Super Panels:

  • Childhood onset leukodystrophy
  • Hypotonic infant
  • Paediatric disorders
  • review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Red
    • BRIDGE study SPEED NEURO Tier1 Gene
    Phenotypes
    • Trichohepatoenteric syndrome 2, 614602
    Tags
    • new-gene-name
    Red SKIV2L in Childhood onset dystonia, chorea or related movement disorder


    Level 2: Neurology
    Version 7.13
    Latest signed off version: v7.0 (30 Apr 2025)

    review Not set
    Sources
    • Expert Review Red
    • London North GLH
    Tags
    • new-gene-name