Atypical haemolytic uraemic syndrome
Gene: VTNEnsemblGeneIds (GRCh38): ENSG00000109072
EnsemblGeneIds (GRCh37): ENSG00000109072
OMIM: 193190, Gene2Phenotype
VTN is in 1 panel
2 reviews
David Kavanagh (Newcastle upon Tyne NHS hospitals trust)
Gene burden testing has identified an enrichment for rare genetic variants in this gene in aHUS.
No familial inheritance described.
Should be regarded as ascertainment study until replication studies validate.Created: 6 Aug 2019, 9:12 a.m. | Last Modified: 6 Aug 2019, 9:12 a.m.
Panel Version: 1.9
Mode of inheritance
Unknown
Phenotypes
aHUS
Publications
Eleanor Williams (Genomics England Curator)
This gene was part of an initial gene list collated by Valerie Wilson, The National Renal Complement Therapeutics Centre, February 2019 on behalf of Yorkshire and North East GLH for the GMS Renal Specialist Test Group; Gene Symbol submitted: VTN; Suggested initial gene rating: none provided;Created: 12 Feb 2019, 12:40 p.m.
Details
- Mode of Inheritance
- Unknown
- Sources
-
- NHS GMS
- Phenotypes
-
- Atypical haemolytic uraemic syndrome
- aHUS
- OMIM
- 193190
- Clinvar variants
- Variants in VTN
- Penetrance
- None
- Publications
- Panels with this gene
History Filter Activity
Set Phenotypes
Eleanor Williams (Genomics England Curator)Phenotypes for gene: VTN were changed from to Atypical haemolytic uraemic syndrome; aHUS
Set publications
Eleanor Williams (Genomics England Curator)Publications for gene: VTN were set to
Set mode of inheritance
Eleanor Williams (Genomics England Curator)Mode of inheritance for gene: VTN was changed from to Unknown
Created, Added New Source, Set mode of inheritance
Eleanor Williams (Genomics England Curator)gene: VTN was added gene: VTN was added to Atypical haemolytic uraemic syndrome. Sources: NHS GMS Mode of inheritance for gene: VTN was set to