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  3. NLGN3
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Autism

Gene: NLGN3

Amber List (moderate evidence)
NLGN3 (neuroligin 3)
EnsemblGeneIds (GRCh38): ENSG00000196338
EnsemblGeneIds (GRCh37): ENSG00000196338
OMIM: 300336, Gene2Phenotype
NLGN3 is in 3 panels

1 review

Louise Daugherty (Genomics England Curator)

I don't know

Each gene in the SFARI Human Gene module has a dedicated entry summary page, see here for more info on this gene: https://gene.sfari.org/database/human-gene/NLGN3
Created: 1 Apr 2019, 11:26 a.m.
Created: 1 Apr 2019, 11:26 a.m.

Panel version: 0.11

Details

Sources
  • Expert Review Amber
  • SFARI
OMIM
300336
Clinvar variants
Variants in NLGN3
Penetrance
None
Publications
Panels with this gene

History Filter Activity

1 Apr 2019, Gel status: 2

Set publications

Louise Daugherty (Genomics England Curator)

Publications for gene NLGN3 were changed from to 20212079; 26185613; 23042784; 24267887; 26166478; 25989142; 24090431; 24581740; 26167905; 23999528; 25294932

29 Mar 2019, Gel status: 2

Added New Source, Status Update

Louise Daugherty (Genomics England Curator)

Source Expert Review Amber was added to NLGN3. Rating Changed from Red List (low evidence) to Amber List (moderate evidence)

29 Mar 2019, Gel status: 1

Created, Added New Source, Set mode of inheritance

Louise Daugherty (Genomics England Curator)

gene: NLGN3 was added gene: NLGN3 was added to Autism. Sources: SFARI Mode of inheritance for gene: NLGN3 was set to