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Intellectual_disability

Gene: INF2

Red List (low evidence)

INF2 (inverted formin, FH2 and WH2 domain containing)
EnsemblGeneIds (GRCh38): ENSG00000203485
EnsemblGeneIds (GRCh37): ENSG00000203485
OMIM: 610982, Gene2Phenotype
INF2 is in 6 panels

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Details

Sources
  • Radboud University Medical Center, Nijmegen
Phenotypes
  • Glomerulosclerosis, focal segmental, 5, 613237Charcot-Marie-Tooth disease, dominant intermediate E, 614455
OMIM
610982
Clinvar variants
Variants in INF2
Penetrance
Complete
Panels with this gene

History Filter Activity

8 Oct 2015, Gel status: 1

Added New Source

Ellen McDonagh (Genomics England Curator)

INF2 was added to Intellectual_disabilitypanel. Sources: Radboud University Medical Center, Nijmegen