Rare multisystem ciliopathy disorders
Gene: SEC63EnsemblGeneIds (GRCh38): ENSG00000025796
EnsemblGeneIds (GRCh37): ENSG00000025796
OMIM: 608648, Gene2Phenotype
SEC63 is in 6 panels
1 review
Alice Gardham (Genomics England)
Comment when marking as ready: Known to cause polycystic liver disease without renal involvement so would not fulfil entry criteria for this gene panelCreated: 25 Jan 2017, 9:36 a.m.
Details
- Mode of Inheritance
- MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
- Sources
-
- Expert Review Red
- UKGTN
- Expert list
- Phenotypes
-
- Polycystic Kidney Disease, Nephronophthisis And Related Disorders 22 Gene Panel
- OMIM
- 608648
- Clinvar variants
- Variants in SEC63
- Penetrance
- Complete
- Panels with this gene
History Filter Activity
panel promoted to version 1
Alice Gardham (Genomics England)Promoted to version 1 by Alice Gardham on 26th January 2017
Gene classified by Genomics England curator
Alice Gardham (Genomics England)This gene has been classified as Red List (Low Evidence).
Upload gene information
Ellen McDonagh (Genomics England Curator)SEC63 was added to Rare multisystem ciliopathy disorderspanel. Sources: UKGTN
Set Phenotypes
Ellen McDonagh (Genomics England Curator)Phenotypes for gene SEC63 were set to Polycystic Kidney Disease, Nephronophthisis And Related Disorders 22 Gene Panel
Added New Source
Ellen McDonagh (Genomics England Curator)SEC63 was added to Rare multisystem ciliopathy disorderspanel. Sources: Expert list
Created
Ellen McDonagh (Genomics England Curator)SEC63 was created by ellenmcdonagh