Ductal plate malformation

Gene: CLDN16

Red List (low evidence)

CLDN16 (claudin 16)
EnsemblGeneIds (GRCh38): ENSG00000113946
EnsemblGeneIds (GRCh37): ENSG00000113946
OMIM: 603959, Gene2Phenotype
CLDN16 is in 9 panels

1 review

Ivone Leong (Genomics England Curator)

Red List (low evidence)

Demoted from amber to red as insufficient evidence
Created: 12 Nov 2018, 1:55 p.m.


Mode of Inheritance
BIALLELIC, autosomal or pseudoautosomal
  • Expert Review Red
  • Radboud University Medical Center, Nijmegen
  • Illumina TruGenome Clinical Sequencing Services
  • Expert list
  • Hypomagnesemia 3, renal (248250)
Clinvar variants
Variants in CLDN16
Panels with this gene

History Filter Activity

30 Nov 2018, Gel status: 1

Panel promoted to version 1.0

Ellen McDonagh (Genomics England Curator)

Ivone Leong: Demoted from amber to red as i

12 Nov 2018, Gel status: 1

Added New Source, Status Update

Ivone Leong (Genomics England Curator)

Source Expert Review Red was added to CLDN16. Rating Changed from Amber List (moderate evidence) to Red List (low evidence)

12 Nov 2018, Gel status: 2

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

Ivone Leong (Genomics England Curator)

gene: CLDN16 was added gene: CLDN16 was added to Ductal plate malformation (DPM). Sources: Expert list,Illumina TruGenome Clinical Sequencing Services,Radboud University Medical Center, Nijmegen Mode of inheritance for gene: CLDN16 was set to BIALLELIC, autosomal or pseudoautosomal Phenotypes for gene: CLDN16 were set to Hypomagnesemia 3, renal (248250)