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  3. PLXNB3
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Intellectual_disability

Gene: PLXNB3

Red List (low evidence)
PLXNB3 (plexin B3)
EnsemblGeneIds (GRCh38): ENSG00000198753
EnsemblGeneIds (GRCh37): ENSG00000198753
OMIM: 300214, Gene2Phenotype
PLXNB3 is in 2 panels

0 reviews

Details

Mode of Inheritance
X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males)
Sources
  • Candidate gene (Grozeva et al, 2015)
Phenotypes
  • Intellectual disability
OMIM
300214
Clinvar variants
Variants in PLXNB3
Penetrance
Complete
Publications
Panels with this gene

History Filter Activity

8 Oct 2015, Gel status: 0

Added New Source

Ellen McDonagh (Genomics England Curator)

PLXNB3 was added to Intellectual_disabilitypanel. Sources: Candidate gene (Grozeva et al, 2015)