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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
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