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Primary immunodeficiency or monogenic inflammatory bowel disease

Gene: GTF3AP5

No list

GTF3AP5 (general transcription factor IIIA pseudogene 5)
EnsemblGeneIds (GRCh38): ENSG00000225816
EnsemblGeneIds (GRCh37): ENSG00000225816
GTF3AP5 is in 1 panel

1 review

Achchuthan Shanmugasundram (Genomics England Curator)

Comment on list classification: PMID:36399538 reports the association of GTF3A to immunodeficiency rather than GTF3AP5. Hence, the reviewer removed their review. This gene is therefore rated grey on this panel.
Created: 15 Aug 2025, 5:49 p.m. | Last Modified: 15 Aug 2025, 5:49 p.m.
Panel Version: 8.34

Details

Mode of Inheritance
BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Removed
Phenotypes
  • PID
Tags
curated_removed
Clinvar variants
Variants in GTF3AP5
Penetrance
None
Publications
Panels with this gene

History Filter Activity

15 Aug 2025, Gel status: 0

Entity classified by Genomics England curator

Achchuthan Shanmugasundram (Genomics England Curator)

Gene: gtf3ap5 has been removed from the panel.

15 Aug 2025, Gel status: 0

Added Tag

Achchuthan Shanmugasundram (Genomics England Curator)

Tag curated_removed tag was added to gene: GTF3AP5.

15 Aug 2025, Gel status: 0

Entity classified by Genomics England curator

Achchuthan Shanmugasundram (Genomics England Curator)

Gene: gtf3ap5 has been removed from the panel.

17 Oct 2024, Gel status: 0

Created, Added New Source, Set mode of inheritance, Set publications, Set Phenotypes

Dmitrijs Rots (Children's Clinical University Hospital)

gene: GTF3AP5 was added gene: GTF3AP5 was added to Primary immunodeficiency or monogenic inflammatory bowel disease. Sources: Literature Mode of inheritance for gene: GTF3AP5 was set to BIALLELIC, autosomal or pseudoautosomal Publications for gene: GTF3AP5 were set to PMID: 36399538 Phenotypes for gene: GTF3AP5 were set to PID Review for gene: GTF3AP5 was set to AMBER