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Intellectual disability

Gene: CNTN3

Red List (low evidence)

CNTN3 (contactin 3)
EnsemblGeneIds (GRCh38): ENSG00000113805
EnsemblGeneIds (GRCh37): ENSG00000113805
OMIM: 601325, Gene2Phenotype
CNTN3 is in 2 panels

1 review

Zornitza Stark (Australian Genomics)

I don't know

One to watch, suggest adding as Red.
Created: 22 Jun 2018, 10:34 a.m.

Mode of inheritance
BIALLELIC, autosomal or pseudoautosomal

Publications

Details

Mode of Inheritance
BIALLELIC, autosomal or pseudoautosomal
Sources
  • Victorian Clinical Genetics Services
OMIM
601325
Clinvar variants
Variants in CNTN3
Penetrance
None
Publications
Panels with this gene

History Filter Activity

28 Sep 2018, Gel status: 1

Added New Source

Louise Daugherty (Genomics England Curator)

Source Victorian Clinical Genetics Services was added to CNTN3.

22 Jun 2018, Gel status: 0

Added New Source

Zornitza Stark (Australian Genomics)

CNTN3 was added to Intellectual disability panel. Sources: Literature

22 Jun 2018, Gel status: 0

Created

Zornitza Stark (Australian Genomics)

CNTN3 was created by Zornitza Stark