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  3. ASB12
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Intellectual_disability

Gene: ASB12

Red List (low evidence)
ASB12 (ankyrin repeat and SOCS box containing 12)
EnsemblGeneIds (GRCh38): ENSG00000198881
EnsemblGeneIds (GRCh37): ENSG00000198881
OMIM: 300891, Gene2Phenotype
ASB12 is in 1 panel

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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
300891
Clinvar variants
Variants in ASB12
Penetrance
Complete
Publications
Panels with this gene

History Filter Activity

8 Oct 2015, Gel status: 0

Added New Source

Ellen McDonagh (Genomics England Curator)

ASB12 was added to Intellectual_disabilitypanel. Sources: Candidate gene (Grozeva et al, 2015)