Monogenic Diabetes
Gene: CIDECEnsemblGeneIds (GRCh38): ENSG00000187288
EnsemblGeneIds (GRCh37): ENSG00000187288
OMIM: 612120, Gene2Phenotype
CIDEC is in 3 panels
1 review
Hali Van Niel (University of Melbourne)
PMID: 20049731 - single individual reported with CIDEC-related familial partial lipodystrophy
none reported with diabetesCreated: 9 May 2024, 3:42 a.m. | Last Modified: 9 May 2024, 3:42 a.m.
Panel Version: 0.107
Mode of inheritance
Unknown
Phenotypes
CIDEC-related familial partial lipodystrophy MONDO:0014098
Publications
Details
- Mode of Inheritance
- BIALLELIC, autosomal or pseudoautosomal
- Sources
-
- Expert Review Red
- Phenotypes
-
- CIDEC-related familial partial lipodystrophy MONDO:0014098
- OMIM
- 612120
- Clinvar variants
- Variants in CIDEC
- Penetrance
- None
- Publications
- Panels with this gene
History Filter Activity
Entity classified by Genomics England curator
Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)Gene: cidec has been classified as Red List (Low Evidence).
Set Phenotypes
Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)Phenotypes for gene: CIDEC were changed from Lipodystrophy, familial partial, type 5 to CIDEC-related familial partial lipodystrophy MONDO:0014098
Created, Added New Source, Set mode of inheritance, Set publications, Set Phenotypes
Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)gene: CIDEC was added gene: CIDEC was added to Monogenic diabetes. Sources: Expert Review Red Mode of inheritance for gene: CIDEC was set to BIALLELIC, autosomal or pseudoautosomal Publications for gene: CIDEC were set to 20049731 Phenotypes for gene: CIDEC were set to Lipodystrophy, familial partial, type 5