Monogenic Diabetes
Gene: NEUROG3
NEUROG3 (neurogenin 3)
EnsemblGeneIds (GRCh38): ENSG00000122859
EnsemblGeneIds (GRCh37): ENSG00000122859
OMIM: 604882, Gene2Phenotype
NEUROG3 is in 5 panels
EnsemblGeneIds (GRCh38): ENSG00000122859
EnsemblGeneIds (GRCh37): ENSG00000122859
OMIM: 604882, Gene2Phenotype
NEUROG3 is in 5 panels
1 review
Hali Van Niel (University of Melbourne)
32574610: review of reported NEOROG3 diabetes cases reports 13 cases type 1 diabetes
Age diabetes onset ranges from neonatal to 24 years (5 neonatal and 8 over 7 years)Created: 23 May 2024, 12:37 a.m. | Last Modified: 23 May 2024, 12:37 a.m.
Panel Version: 0.125
Mode of inheritance
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
congenital malabsorptive diarrhea 4 MONDO:0012479
Publications
Details
- Mode of Inheritance
- BIALLELIC, autosomal or pseudoautosomal
- Sources
-
- Expert Review Green
- UKGTN
- Phenotypes
-
- congenital malabsorptive diarrhea 4 MONDO:0012479
- OMIM
- 604882
- Clinvar variants
- Variants in NEUROG3
- Penetrance
- None
- Publications
- Panels with this gene
History Filter Activity
23 May 2024, Gel status: 3
Entity classified by Genomics England curator
Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)Gene: neurog3 has been classified as Green List (High Evidence).
23 May 2024, Gel status: 3
Set Phenotypes
Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)Phenotypes for gene: NEUROG3 were changed from to congenital malabsorptive diarrhea 4 MONDO:0012479
17 Jan 2020, Gel status: 3
Created, Added New Source, Set mode of inheritance, Set publications
Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)gene: NEUROG3 was added gene: NEUROG3 was added to Monogenic diabetes. Sources: UKGTN,Expert Review Green Mode of inheritance for gene: NEUROG3 was set to BIALLELIC, autosomal or pseudoautosomal Publications for gene: NEUROG3 were set to 25650326; 26288179