IUGR and IGF abnormalities
Gene: CUL7
CUL7 (cullin 7)
EnsemblGeneIds (GRCh38): ENSG00000044090
EnsemblGeneIds (GRCh37): ENSG00000044090
OMIM: 609577, Gene2Phenotype
CUL7 is in 7 panels
EnsemblGeneIds (GRCh38): ENSG00000044090
EnsemblGeneIds (GRCh37): ENSG00000044090
OMIM: 609577, Gene2Phenotype
CUL7 is in 7 panels
4 reviews
Mehul Dattani (UCL Institute of Child Health)
Philip Murray (University of Manchester)
Peter Clayton (University of Manchester)
Rebecca Foulger (Genomics England curator)
Comment on phenotypes: Updated phenotype field to include current OMIM disorder and ID (MIM:273750)Created: 17 Aug 2017, 9:36 a.m.
Details
- Mode of Inheritance
- BIALLELIC, autosomal or pseudoautosomal
- Sources
-
- Expert Review Green
- Emory Genetics Laboratory
- Phenotypes
-
- 3-M syndrome 1, 273750
- OMIM
- 609577
- Clinvar variants
- Variants in CUL7
- Penetrance
- Complete
- Panels with this gene
History Filter Activity
17 Aug 2017, Gel status: 4
Set Phenotypes
Rebecca Foulger (Genomics England curator)Phenotypes for CUL7 were set to 3-M syndrome 1, 273750
3 Apr 2016, Gel status: 4
Gene classified by Genomics England curator
emma baple (Genomics England Curator)This gene has been classified as Green List (High Evidence).
3 Apr 2016, Gel status: 4
Set Phenotypes
emma baple (Genomics England Curator)Phenotypes for CUL7 were set to 3M syndrome
3 Apr 2016, Gel status: 4
Set Mode of Inheritance
emma baple (Genomics England Curator)Mode of inheritance for CUL7 was changed to BIALLELIC, autosomal or pseudoautosomal
3 Apr 2016, Gel status: 4
Gene classified by Genomics England curator
emma baple (Genomics England Curator)This gene has been classified as Green List (High Evidence).
28 Apr 2015, Gel status: 1
Added New Source
GEL ()CUL7 was added to IUGR and IGF abnormalitiespanel. Sources: Emory Genetics Laboratory