Proteinuria
Gene: TNS2
TNS2 (tensin 2)
EnsemblGeneIds (GRCh38): ENSG00000111077
EnsemblGeneIds (GRCh37): ENSG00000111077
OMIM: 607717, Gene2Phenotype
TNS2 is in 2 panels
EnsemblGeneIds (GRCh38): ENSG00000111077
EnsemblGeneIds (GRCh37): ENSG00000111077
OMIM: 607717, Gene2Phenotype
TNS2 is in 2 panels
1 review
Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)
Five families reported in this paper reporting multiple new SRNS genes.
Sources: Expert listCreated: 9 Jan 2020, 3:56 a.m.
Mode of inheritance
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Nephrotic syndrome
Publications
Details
- Mode of Inheritance
- BIALLELIC, autosomal or pseudoautosomal
- Sources
-
- Expert Review Green
- Expert list
- Phenotypes
-
- Nephrotic syndrome
- OMIM
- 607717
- Clinvar variants
- Variants in TNS2
- Penetrance
- None
- Publications
- Panels with this gene
History Filter Activity
9 Jan 2020, Gel status: 3
Entity classified by Genomics England curator
Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)Gene: tns2 has been classified as Green List (High Evidence).
9 Jan 2020, Gel status: 3
Entity classified by Genomics England curator
Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)Gene: tns2 has been classified as Green List (High Evidence).
9 Jan 2020, Gel status: 1
Created, Added New Source, Set mode of inheritance, Set publications, Set Phenotypes
Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)gene: TNS2 was added gene: TNS2 was added to Proteinuria_VCGS_KidGen. Sources: Expert list Mode of inheritance for gene: TNS2 was set to BIALLELIC, autosomal or pseudoautosomal Publications for gene: TNS2 were set to 29773874 Phenotypes for gene: TNS2 were set to Nephrotic syndrome Review for gene: TNS2 was set to GREEN