Kidneyome_SuperPanel_KidGen_VCGS
Gene: CD151EnsemblGeneIds (GRCh38): ENSG00000177697
EnsemblGeneIds (GRCh37): ENSG00000177697
OMIM: 602243, Gene2Phenotype
CD151 is in 7 panels
0 reviews
Details
- Mode of Inheritance
- BIALLELIC, autosomal or pseudoautosomal
- Sources
-
- Expert Review Green
- Expert list
- Victorian Clinical Genetics Services
- Phenotypes
-
- Nephropathy with pretibial epidermolysis bullosa and deafness, MIM#609057
- OMIM
- 602243
- Clinvar variants
- Variants in CD151
- Penetrance
- None
- Publications
- Panels with this gene
History Filter Activity
Added New Source, Set Phenotypes, Status Update
Ivone Leong (Genomics England Curator)Source Expert Review Green was added to CD151. Added phenotypes Nephropathy with pretibial epidermolysis bullosa and deafness, MIM#609057 for gene: CD151 Rating Changed from Red List (low evidence) to Green List (high evidence)
Added New Source, Set Phenotypes, Status Update
Ivone Leong (Genomics England Curator)Source Expert Review Red was added to CD151. Added phenotypes Nephropathy with pretibial epidermolysis bullosa and deafness, MIM#609057 for gene: CD151 Rating Changed from Green List (high evidence) to Red List (low evidence)
Added New Source, Set mode of inheritance, Set Phenotypes, Set publications
Ivone Leong (Genomics England Curator)Source Expert list was added to CD151. Mode of inheritance for gene CD151 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal Added phenotypes Nephropathy with pretibial epidermolysis bullosa and deafness, MIM#609057 for gene: CD151 Publications for gene CD151 were changed from to 15265795; 29138120
Created, Added New Source, Set mode of inheritance
Ivone Leong (Genomics England Curator)gene: CD151 was added gene: CD151 was added to Kidneyome_SuperPanel_KidGen_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services Mode of inheritance for gene: CD151 was set to Unknown