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 1.181

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


Level 2: Fetal (including NIPD)
Version 6.140
Latest signed off version: v6.0 (30 Apr 2025)

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

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 2: Audiology
    Version 5.57
    Latest signed off version: v5.0 (30 Apr 2025)

    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


    Level 2: Developmental disorders
    Version 7.31
    Latest signed off version: v7.0 (30 Apr 2025)

    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