TRPC6 transient receptor potential cation channel subfamily C member 6
Information
- Symbol
- TRPC6
- Type
- protein-coding
- Description
- transient receptor potential cation channel subfamily C member 6
- Entrez Gene ID
- 7225
- Genome
- hg19
- Position
- chr11:101,322,295-101,454,738
- Genome
- hg38
- Position
- chr11:101,451,564-101,584,007
- MIM
- 603652 OMIM
- HGNC
- HGNC:12338 HGNC
- Ensembl
- ENSG00000137672 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Pathogenic | 2 | 14 |
Likely pathogenic | 0 | 30 |
Benign | 10 | 132 |
Likely benign | 0 | 188 |
Conflicting classifications of pathogenicity | 0 | 26 |
drug response | 0 | 72 |
Uncertain significance | 0 | 354 |
Ranking
ClinVar | |
---|---|
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0 |
![]() |
0 |
![]() |
106 |
![]() |
560 |
![]() |
102 |
Frequency
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
Disease area statistics
Locus Zoom
Variants
Search Word
Target data | : |
MGeND data only
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Category | : |
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Search word | : | |
Filtering | : |
Variant name | Gene | AA change | CDS | Japanese frequency |
TogoVar | MGeND | Genome | ClinVar | CIViC evidence | DisGeNET entry | COSMIC occurrence |
Prediction | |||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Entry | Origin | Type | Annotation | Entry | Origin | Annotation |
Search Word
Target data | : |
MGeND data only
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Category | : |
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Search word | : | |
Filtering | : |
Name | MGeND | Type | Genome | Size | Chromosome | Start | Stop | Ref | Alt | ClinVar | Origin | Entry | CIViC evidence | DisGeNET entry | |||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Entry | Origin | Type | Annotation |
Search Word
Target data | : |
MGeND data only
|
Category | : |
|
Search word | : | |
Filtering | : |
Name | MGeND | Type | Genome | Gene symbol | Chromosome | Genomic start | Genomic stop | Strand | Ref | Alt | ClinVar | Origin | Entry | CIViC evidence | DisGeNET entry | |||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Entry | Origin | Type | Annotation |
Type | ID |
---|---|
SYNONYM | FSGS2 |
SYNONYM | TRP6 |
MIM | 603652 OMIM |
HGNC | HGNC:12338 HGNC |
Ensembl | ENSG00000137672 Ensembl |
AllianceGenome | HGNC:12338 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000348423.8 | hg38 | chr11 | 101,452,955 | 101,583,503 | 130,549 |
ENST00000360497.4 | hg38 | chr11 | 101,452,955 | 101,583,503 | 130,549 |
ENST00000532133.5 | hg38 | chr11 | 101,452,872 | 101,583,506 | 130,635 |
ENST00000344327.8 | hg38 | chr11 | 101,451,564 | 101,584,007 | 132,444 |
ENST00000344327.8 | hg19 | chr11 | 101,322,295 | 101,454,738 | 132,444 |
ENST00000532133.5 | hg19 | chr11 | 101,323,603 | 101,454,237 | 130,635 |
ENST00000348423.8 | hg19 | chr11 | 101,323,686 | 101,454,234 | 130,549 |
ENST00000360497.4 | hg19 | chr11 | 101,323,686 | 101,454,234 | 130,549 |
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