Transplant Co-Morbidity Superpanel
Gene: INSEnsemblGeneIds (GRCh38): ENSG00000254647
EnsemblGeneIds (GRCh37): ENSG00000254647
OMIM: 176730, Gene2Phenotype
INS is in 7 panels
0 reviews
Details
- Mode of Inheritance
- BOTH monoallelic and biallelic, autosomal or pseudoautosomal
- Sources
-
- Expert Review Green
- NHS GMS
- Phenotypes
-
- Maturity Onset Diabetes of the Young (Dominant)
- Diabetes mellitus, type 1, 125852
- Diabetes mellitus, insulin-dependent, 2, 125852
- Transient Neonatal Diabetes, Dominant/Recessive
- MATURITY-ONSET DIABETES OF THE YOUNG, TYPE 10
- Maturity-onset diabetes of the young, type 10, 613370
- Diabetes mellitus, permanent neonatal, 606176
- Hyperproinsulinemia, familial, with or without diabetes
- Permanent Neonatal diabetes mellitus
- Maturity Onset Diabetes of the Young
- MODY10
- OMIM
- 176730
- Clinvar variants
- Variants in INS
- Penetrance
- None
- Panels with this gene
History Filter Activity
Created, Added New Source, Set mode of inheritance, Set Phenotypes
Bryony Thompson (Royal Melbourne Hospital)gene: INS was added gene: INS was added to Transplant Co-Morbidity Superpanel. Sources: NHS GMS,Expert Review Green Mode of inheritance for gene: INS was set to BOTH monoallelic and biallelic, autosomal or pseudoautosomal Phenotypes for gene: INS were set to Maturity Onset Diabetes of the Young (Dominant); Diabetes mellitus, type 1, 125852; Diabetes mellitus, insulin-dependent, 2, 125852; Transient Neonatal Diabetes, Dominant/Recessive; MATURITY-ONSET DIABETES OF THE YOUNG, TYPE 10; Maturity-onset diabetes of the young, type 10, 613370; Diabetes mellitus, permanent neonatal, 606176; Hyperproinsulinemia, familial, with or without diabetes; Permanent Neonatal diabetes mellitus; Maturity Onset Diabetes of the Young; MODY10