Multi-organ autoimmune diabetes
Gene: IER3IP1EnsemblGeneIds (GRCh38): ENSG00000134049
EnsemblGeneIds (GRCh37): ENSG00000134049
OMIM: 609382, Gene2Phenotype
IER3IP1 is in 16 panels
2 reviews
Ellen McDonagh (Genomics England Curator)
Comment on list classification: Removed due to expert review.Created: 22 Jul 2016, 3:09 p.m.
Sian Ellard (University of Exeter Medical School)
Remove gene from panelCreated: 8 Dec 2015, 2:32 p.m.
Details
- Sources
-
- Expert Review Removed
- UKGTN
- Phenotypes
-
- Neonatal Diabetes
- Tags
- OMIM
- 609382
- Clinvar variants
- Variants in IER3IP1
- Penetrance
- Complete
- Panels with this gene
-
- Possible mitochondrial disorder, nuclear genes
- Mitochondrial disorders
- Intellectual disability
- Fetal anomalies
- Early onset or syndromic epilepsy
- Paediatric disorders - additional genes
- Dystonia, chorea or related movement disorder, childhood onset
- Undiagnosed metabolic disorders
- Severe microcephaly
- Diabetes with additional phenotypes suggestive of a monogenic aetiology
- Monogenic diabetes
- Neonatal diabetes
- Likely inborn error of metabolism
- Familial diabetes
- Multi-organ autoimmune diabetes
- DDG2P
History Filter Activity
Added Tag
Arina Puzriakova (Genomics England Curator)Tag curated_removed tag was added to gene: IER3IP1.
panel promoted to version 1
Ellen McDonagh (Genomics England Curator)25th July 2016: Panel revised acccording to expert review, further evidence sources and comparison with the Familial Diabetes version 1 panel. Promoted to version 1.
Gene classified by Genomics England curator
Ellen McDonagh (Genomics England Curator)This gene has been removed from the panel.
Gene classified by Genomics England curator
Ellen McDonagh (Genomics England Curator)This gene has been removed from the panel.
Added New Source
Ellen McDonagh (Genomics England Curator)IER3IP1 was added to Multi-organ autoimmune diabetespanel. Sources: UKGTN