Familial Neural Tube Defects

Gene: FUZ

Red List (low evidence)

FUZ (fuzzy planar cell polarity protein)
EnsemblGeneIds (GRCh38): ENSG00000010361
EnsemblGeneIds (GRCh37): ENSG00000010361
OMIM: 610622, Gene2Phenotype
FUZ is in 3 panels

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Details

Sources
  • Radboud University Medical Center, Nijmegen
Phenotypes
  • Neural tube defects
OMIM
610622
Clinvar variants
Variants in FUZ
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.

22 Sep 2016, Gel status: 0

Created

Olivia Niblock (Genomics England Curator)

FUZ was created by oniblock

22 Sep 2016, Gel status: 1

Added New Source

Olivia Niblock (Genomics England Curator)

FUZ was added to Familial Neural Tube Defectspanel. Sources: Radboud University Medical Center, Nijmegen