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  3. ZNF292
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Autism

Gene: ZNF292

Green List (high evidence)
ZNF292 (zinc finger protein 292)
EnsemblGeneIds (GRCh38): ENSG00000188994
EnsemblGeneIds (GRCh37): ENSG00000188994
OMIM: 616213, Gene2Phenotype
ZNF292 is in 2 panels

2 reviews

Sarah Leigh (Genomics England Curator)

Green List (high evidence)

Associated with relevant phenotype in OMIM and as strong Gen2Phen gene. At least seven autosomal dominant or de novo ZNF292 variants have been reported in at least eleven unrelated cases of Intellectual developmental disorder, autosomal dominant 64 (OMIM: 619188)(PMID: 31723249).
Created: 10 Jan 2023, 12:52 p.m. | Last Modified: 10 Jan 2023, 12:52 p.m.
Panel Version: 0.24
Created: 10 Jan 2023, 12:52 p.m.
Last Modified: 10 Jan 2023, 12:52 p.m.
Panel version: 0.24

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/ZNF292
Created: 1 Apr 2019, 11:26 a.m.
Created: 1 Apr 2019, 11:26 a.m.

Panel version: 0.11

Details

Mode of Inheritance
MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Sources
  • Expert Review Green
  • SFARI
Phenotypes
  • Intellectual developmental disorder, autosomal dominant 64, OMIM:619188
  • intellectual developmental disorder, autosomal dominant 64, MONDO:0030934
OMIM
616213
Clinvar variants
Variants in ZNF292
Penetrance
None
Publications
Panels with this gene

History Filter Activity

10 Jan 2023, Gel status: 3

Set publications

Sarah Leigh (Genomics England Curator)

Publications for gene: ZNF292 were set to

10 Jan 2023, Gel status: 3

Entity classified by Genomics England curator

Sarah Leigh (Genomics England Curator)

Gene: znf292 has been classified as Green List (High Evidence).

10 Jan 2023, Gel status: 1

Set mode of inheritance

Sarah Leigh (Genomics England Curator)

Mode of inheritance for gene: ZNF292 was changed from to MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown

10 Jan 2023, Gel status: 1

Set Phenotypes

Sarah Leigh (Genomics England Curator)

Phenotypes for gene: ZNF292 were changed from to Intellectual developmental disorder, autosomal dominant 64, OMIM:619188; intellectual developmental disorder, autosomal dominant 64, MONDO:0030934

29 Mar 2019, Gel status: 1

Added New Source

Louise Daugherty (Genomics England Curator)

Source Expert Review Red was added to ZNF292.

29 Mar 2019, Gel status: 1

Created, Added New Source, Set mode of inheritance

Louise Daugherty (Genomics England Curator)

gene: ZNF292 was added gene: ZNF292 was added to Autism. Sources: SFARI Mode of inheritance for gene: ZNF292 was set to