Coarse facial features including Coffin-Siris-like disorders
Gene: INSREnsemblGeneIds (GRCh38): ENSG00000171105
EnsemblGeneIds (GRCh37): ENSG00000171105
OMIM: 147670, Gene2Phenotype
INSR is in 13 panels
2 reviews
Alice Gardham (Genomics England)
Comment when marking as ready: Exclusion criteria include insulin resistance so not relevant for this panelCreated: 23 Nov 2016, 10:39 a.m.
Alice Gardham (North West Thames Genetics)
Mode of inheritance
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Rabson-Mendenhall syndrome 262190, Donohue 246200
Details
- Mode of Inheritance
- BIALLELIC, autosomal or pseudoautosomal
- Sources
-
- Expert Review Red
- Phenotypes
-
- Rabson-Mendenhall syndrome 262190, Donohue syndrome 246200
- OMIM
- 147670
- Clinvar variants
- Variants in INSR
- Penetrance
- Complete
- Publications
- Panels with this gene
-
- Osteogenesis imperfecta
- Multi-organ autoimmune diabetes
- Lipodystrophy - childhood onset
- IUGR and IGF abnormalities
- Monogenic diabetes
- Intellectual disability
- Insulin resistance (including lipodystrophy)
- Monogenic short stature
- Familial diabetes
- Neonatal diabetes
- Fetal anomalies
- Diabetes with additional phenotypes suggestive of a monogenic aetiology
- Congenital hyperinsulinism
History Filter Activity
Gene classified by Genomics England curator
Alice Gardham (Genomics England)This gene has been classified as Red List (Low Evidence).
Approved Gene
Ellen McDonagh (Genomics England Curator)This proposed gene was validated and added to this panel
Created
Alice Gardham (North West Thames Genetics)INSR was created by alicegardham
Added New Source
Alice Gardham (North West Thames Genetics)INSR was added to Coarse facial features including Coffin-Siris-like disorderspanel. Sources: UKGTN