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  2. Renal and urinary tract disorders
  3. GLIS2
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Renal and urinary tract disorders

Gene: GLIS2

Red List (low evidence)
GLIS2 (GLIS family zinc finger 2)
EnsemblGeneIds (GRCh38): ENSG00000126603
EnsemblGeneIds (GRCh37): ENSG00000126603
OMIM: 608539, Gene2Phenotype
GLIS2 is in 11 panels

2 reviews

Ellen Thomas (Genomics England Curator)

Comment on list classification: Insufficient evidence - await further research results.
Created: 10 May 2016, 10:21 a.m.
Created: 10 May 2016, 10:21 a.m.

Panel version: Imported from Cystic kidney disease panel version 0.25

Miranda Durkie (Genetics)

Green List (high evidence)

Nephronophthisis (AR)
Created: 22 Oct 2015, 11:19 a.m.

Mode of inheritance
BIALLELIC, autosomal or pseudoautosomal

Created: 22 Oct 2015, 11:19 a.m.

Panel version: Imported from Cystic kidney disease panel version 0

History Filter Activity

30 Jan 2019, Gel status: 1

Panel promoted to version 1.0

Eleanor Williams (Genomics England Curator)

Miranda Durkie: Nephronophthisis (AR)

20 Dec 2018, Gel status: 1

Set Phenotypes

Ellen McDonagh (Genomics England Curator)

Added phenotypes Ciliopathy genes associated with cystic kidney disease for gene: GLIS2

20 Dec 2018, Gel status: 1

Created, Added New Source, Set mode of inheritance, Set Phenotypes

Ellen McDonagh (Genomics England Curator)

gene: GLIS2 was added gene: GLIS2 was added to Renal and urinary tract disorders. Sources: Expert Review Red Mode of inheritance for gene: GLIS2 was set to Unknown Phenotypes for gene: GLIS2 were set to Ciliopathy genes associated with cystic kidney disease