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Intellectual_disability

Gene: GPHN

Red List (low evidence)

GPHN (gephyrin)
EnsemblGeneIds (GRCh38): ENSG00000171723
EnsemblGeneIds (GRCh37): ENSG00000171723
OMIM: 603930, Gene2Phenotype
GPHN is in 6 panels

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Details

Sources
  • Radboud University Medical Center, Nijmegen
Phenotypes
  • Molybdenum cofactor deficiency, type C, 252150
OMIM
603930
Clinvar variants
Variants in GPHN
Penetrance
Complete
Panels with this gene

History Filter Activity

8 Oct 2015, Gel status: 1

Added New Source

Ellen McDonagh (Genomics England Curator)

GPHN was added to Intellectual_disabilitypanel. Sources: Radboud University Medical Center, Nijmegen