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
- Undiagnosed metabolic disorders
- DDG2P
- Early onset or syndromic epilepsy
- Paediatric disorders - additional genes
- Diabetes with additional phenotypes suggestive of a monogenic aetiology
- Monogenic diabetes
- Neonatal diabetes
- Likely inborn error of metabolism
- Dystonia, chorea or related movement disorder, childhood onset
- Familial diabetes
- Multi-organ autoimmune diabetes
- Fetal anomalies
- Mitochondrial disorders
- Severe microcephaly
- Intellectual disability
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