1. Genes and Genomic Entities
  2. GREB1L

GREB1L

growth regulation by estrogen in breast cancer 1 like
Gene2Phenotype

5 panels

Panel Reviews Mode of inheritance Details
5 panels
Green GREB1L in CAKUT

Level 3: Structural renal and urinary tract disease
Level 2: Renal and urinary tract disorders
Version 1.175

Component of the following Super Panels:

  • Renal superpanel - broad
  • Renal superpanel - narrow

    		•  review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Expert Review Green
    • Expert list
    Phenotypes
    • Renal hypodysplasia/aplasia 3, 617805
    Tags
    • gene-checked
    Green GREB1L in Fetal anomalies


    Version 3.155
    Latest signed off version: v3.0 (22 Mar 2023)

    		review MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
    Sources
    • Expert Review Green
    • Literature
    Phenotypes
    • Renal hypodysplasia/aplasia 3, OMIM:617805
    • Renal agenesis, MONDO:0018470
    Tags
    • gene-checked
    Green GREB1L in DDG2P


    Version 3.87
    Latest signed off version: v3.1 (22 Mar 2023)

    Component of the following Super Panels:

  • Paediatric disorders

    		•  review MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
    Sources
    • DD-Gene2Phenotype
    • Expert Review Green
    Phenotypes
    • Renal hypodysplasia/aplasia 3, OMIM:617805
    Tags
    • gene-checked
    Green GREB1L in Monogenic hearing loss

    Level 3: Non-syndromic hearing loss
    Level 2: Hearing and ear disorders
    Version 4.36
    Latest signed off version: v4.0 (22 Mar 2023)

    Component of the following Super Panels:

  • Paediatric disorders

    		•  review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Expert Review Green
    • NHS GMS
    • Literature
    Phenotypes
    • Deafness, autosomal dominant 80 OMIM:619274
    • deafness, autosomal dominant 80, MONDO:0030998
    Tags
    • gene-checked
    Green GREB1L in Paediatric disorders - additional genes


    Version 3.9
    Latest signed off version: v3.0 (22 Mar 2023)

    Component of the following Super Panels:

  • Paediatric disorders

    		•  review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Expert Review Green
    • Other
    Phenotypes
    • CAKUT
    • Renal hypodysplasia/aplasia 3, 617805
    • inner ear malformations
    Tags
    • gene-checked