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  3. UBN2
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Autism

Gene: UBN2

Amber List (moderate evidence)
UBN2 (ubinuclein 2)
EnsemblGeneIds (GRCh38): ENSG00000157741
EnsemblGeneIds (GRCh37): ENSG00000157741
OMIM: 613841, Gene2Phenotype
UBN2 is in 0 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/UBN2
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
613841
Clinvar variants
Variants in UBN2
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 UBN2 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 UBN2. 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: UBN2 was added gene: UBN2 was added to Autism. Sources: SFARI Mode of inheritance for gene: UBN2 was set to