PanelApp
  1. Genes and Genomic Entities
  2. GLIS3

GLIS3

GLIS family zinc finger 3
OMIM: 610192, Gene2Phenotype

9 panels

Panel Reviews Mode of inheritance Details
9 panels

Green GLIS3 in Mendeliome


Version 1.3499

1 review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Victorian Clinical Genetics Services
Phenotypes
  • Diabetes mellitus, neonatal, with congenital hypothyroidism, MIM#610199

Green GLIS3 in Intellectual disability syndromic and non-syndromic


Level 2: Neurology and neurodevelopmental disorders
Version 1.398

1 review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Genetic Health Queensland
Phenotypes
  • Diabetes mellitus, neonatal, with congenital hypothyroidism, MIM#610199

Green GLIS3 in Monogenic Diabetes


Level 2: Endocrine disorders
Version 0.152

Component of the following Super Panels:

  • Metabolic Disorders Superpanel

    		•  1 review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • UKGTN
    Phenotypes
    • neonatal diabetes mellitus with congenital hypothyroidism MONDO:0012436

    Green GLIS3 in Mackenzie's Mission_Reproductive Carrier Screening


    Level 2: Screening
    Version 0.110

    		0 reviews BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • Mackenzie's Mission
    Phenotypes
    • Diabetes mellitus, neonatal, with congenital hypothyroidism, 610199 (3)

    Red GLIS3 in Additional findings_Paediatric


    Level 2: Screening
    Version 0.278

    		0 reviews BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Red
    • BabySeq Category C gene
    Phenotypes
    • Diabetes mellitus, neonatal, with congenital hypothyroidism

    Green GLIS3 in Congenital hypothyroidism

    Level 3: Thyroid disorders
    Level 2: Endocrine disorders
    Version 0.53

    		1 review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • Genomics England PanelApp
    Phenotypes
    • Diabetes mellitus, neonatal, with congenital hypothyroidism, MIM# 610199

    Green GLIS3 in Fetal anomalies


    Version 1.465

    		1 review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • Genomics England PanelApp
    • Genetic Health Queensland
    Phenotypes
    • Diabetes mellitus, neonatal, with congenital hypothyroidism, MIM#610199

    Green GLIS3 in Prepair 1000+


    Level 2: Screening
    Version 2.14

    		1 review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • Mackenzie's Mission
    Phenotypes
    • Diabetes mellitus, neonatal, with congenital hypothyroidism MIM#610199

    Green GLIS3 in Genomic newborn screening: BabyScreen+


    Level 2: Screening
    Version 1.140

    		2 reviews BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • BabySeq Category C gene
    • BeginNGS
    Phenotypes
    • Diabetes mellitus, neonatal, with congenital hypothyroidism MIM#610199
    Tags
    • treatable
    • endocrine