|
| Entrez Id: |
7225 |
| Gene Symbol: |
TRPC6 |
TRPC6
|
0.900 |
GeneticVariation
|
disease |
UNIPROT |
TRPC6 G757D Loss-of-Function Mutation Associates with FSGS.
|
26892346 |
2016 |
|
| Entrez Id: |
7225 |
| Gene Symbol: |
TRPC6 |
TRPC6
|
0.900 |
GeneticVariation
|
disease |
UNIPROT |
Mutations in the INF2 gene account for a significant proportion of familial but not sporadic focal and segmental glomerulosclerosis.
|
23014460 |
2013 |
|
| Entrez Id: |
7225 |
| Gene Symbol: |
TRPC6 |
TRPC6
|
0.900 |
GeneticVariation
|
disease |
UNIPROT |
New TRPC6 gain-of-function mutation in a non-consanguineous Dutch family with late-onset focal segmental glomerulosclerosis.
|
23291369 |
2013 |
|
| Entrez Id: |
7225 |
| Gene Symbol: |
TRPC6 |
TRPC6
|
0.900 |
GeneticVariation
|
disease |
UNIPROT |
Mutations in podocyte genes are a rare cause of primary FSGS associated with ESRD in adult patients.
|
22732337 |
2012 |
|
| Entrez Id: |
7225 |
| Gene Symbol: |
TRPC6 |
TRPC6
|
0.900 |
GeneticVariation
|
disease |
UNIPROT |
TRPC6 gene variants in Turkish children with steroid-resistant nephrotic syndrome.
|
21511817 |
2012 |
|
| Entrez Id: |
7225 |
| Gene Symbol: |
TRPC6 |
TRPC6
|
0.900 |
GeneticVariation
|
disease |
UNIPROT |
TRPC6 mutations in children with steroid-resistant nephrotic syndrome and atypical phenotype.
|
21734084 |
2011 |
|
| Entrez Id: |
7225 |
| Gene Symbol: |
TRPC6 |
TRPC6
|
0.900 |
GeneticVariation
|
disease |
UNIPROT |
Immunosuppression and renal outcome in congenital and pediatric steroid-resistant nephrotic syndrome.
|
20798252 |
2010 |
|
| Entrez Id: |
7225 |
| Gene Symbol: |
TRPC6 |
TRPC6
|
0.900 |
GeneticVariation
|
disease |
UNIPROT |
A novel TRPC6 mutation that causes childhood FSGS.
|
19936226 |
2009 |
|
| Entrez Id: |
7225 |
| Gene Symbol: |
TRPC6 |
TRPC6
|
0.900 |
GeneticVariation
|
disease |
UNIPROT |
TRPC6 mutational analysis in a large cohort of patients with focal segmental glomerulosclerosis.
|
19458060 |
2009 |
|
| Entrez Id: |
7225 |
| Gene Symbol: |
TRPC6 |
TRPC6
|
0.900 |
GeneticVariation
|
disease |
UNIPROT |
A mutation in the TRPC6 cation channel causes familial focal segmental glomerulosclerosis.
|
15879175 |
2005 |
|
| Entrez Id: |
7225 |
| Gene Symbol: |
TRPC6 |
TRPC6
|
0.900 |
GeneticVariation
|
disease |
UNIPROT |
TRPC6 is a glomerular slit diaphragm-associated channel required for normal renal function.
|
15924139 |
2005 |
|
| Entrez Id: |
7225 |
| Gene Symbol: |
TRPC6 |
TRPC6
|
0.900 |
GeneticVariation
|
disease |
CLINVAR |
|
|
|
|
| Entrez Id: |
7225 |
| Gene Symbol: |
TRPC6 |
TRPC6
|
0.900 |
Biomarker
|
disease |
CTD_human |
|
|
|
|
| Entrez Id: |
7225 |
| Gene Symbol: |
TRPC6 |
TRPC6
|
0.900 |
Biomarker
|
disease |
GENOMICS_ENGLAND |
|
|
|
|
| Entrez Id: |
7225 |
| Gene Symbol: |
TRPC6 |
TRPC6
|
0.900 |
Biomarker
|
disease |
MGD |
|
|
|
|
| Entrez Id: |
7225 |
| Gene Symbol: |
TRPC6 |
TRPC6
|
0.900 |
CausalMutation
|
disease |
CLINVAR |
|
|
|