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  2. Familial Neural Tube Defects
  3. CDON
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Familial Neural Tube Defects

Gene: CDON

Red List (low evidence)
CDON (cell adhesion associated, oncogene regulated)
EnsemblGeneIds (GRCh38): ENSG00000064309
EnsemblGeneIds (GRCh37): ENSG00000064309
OMIM: 608707, Gene2Phenotype
CDON is in 7 panels

0 reviews

Details

Mode of Inheritance
MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Sources
  • Expert Review Red
  • Radboud University Medical Center, Nijmegen
  • Illumina TruGenome Clinical Sequencing Services
Phenotypes
  • Holoprosencephaly
OMIM
608707
Clinvar variants
Variants in CDON
Penetrance
Complete
Panels with this gene

History Filter Activity

25 Oct 2016, Gel status: 1

panel promoted to version 1

Ellen McDonagh (Genomics England Curator)

25th Oct 2016: This panel was discussed internally, and as Neural tube defects (NTDs) are common multifactorial disorders caused by multiple genes and environmental factors, all genes on this panel should be considered red at this stage. Ready to promote to Version 1.

25 Oct 2016, Gel status: 1

Gene classified by Genomics England curator

Ellen McDonagh (Genomics England Curator)

This gene has been classified as Red List (Low Evidence).

22 Sep 2016, Gel status: 2

Added New Source

Olivia Niblock (Genomics England Curator)

CDON was added to Familial Neural Tube Defectspanel. Source: Radboud University Medical Center, Nijmegen

22 Sep 2016, Gel status: 0

Created

Olivia Niblock (Genomics England Curator)

CDON was created by oniblock

22 Sep 2016, Gel status: 1

Added New Source

Olivia Niblock (Genomics England Curator)

CDON was added to Familial Neural Tube Defectspanel. Sources: Illumina TruGenome Clinical Sequencing Services