KCNK7 potassium two pore domain channel subfamily K member 7
Information
- Symbol
- KCNK7
- Type
- protein-coding
- Description
- potassium two pore domain channel subfamily K member 7
- Entrez Gene ID
- 10089
- Genome
- hg19
- Position
- chr11:65,360,307-65,363,271
- Genome
- hg38
- Position
- chr11:65,592,836-65,595,800
- MIM
- 603940 OMIM
- HGNC
- HGNC:6282 HGNC
- Ensembl
- ENSG00000173338 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| Benign | 0 | 4 |
| Likely benign | 0 | 6 |
| Uncertain significance | 0 | 32 |
Ranking
| ClinVar | |
|---|---|
 |
0 |
 |
0 |
 |
0 |
 |
42 |
 |
0 |
Frequency
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
Disease area statistics
[No Data.]
Locus Zoom
Variants
Search Word
| Target data | : |
MGeND data only
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| 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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| 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
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| Category | : |
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| 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 | K2p7.1 |
| SYNONYM | TWIK3 |
| MIM | 603940 OMIM |
| HGNC | HGNC:6282 HGNC |
| Ensembl | ENSG00000173338 Ensembl |
| AllianceGenome | HGNC:6282 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000342202.8 | hg38 | chr11 | 65,592,855 | 65,595,808 | 2,954 |
| ENST00000394216.6 | hg38 | chr11 | 65,592,855 | 65,595,996 | 3,142 |
| ENST00000394217.6 | hg38 | chr11 | 65,592,855 | 65,595,996 | 3,142 |
| ENST00000340313.5 | hg38 | chr11 | 65,592,836 | 65,595,800 | 2,965 |
| ENST00000340313.5 | hg19 | chr11 | 65,360,307 | 65,363,271 | 2,965 |
| ENST00000342202.8 | hg19 | chr11 | 65,360,326 | 65,363,279 | 2,954 |
| ENST00000394216.6 | hg19 | chr11 | 65,360,326 | 65,363,467 | 3,142 |
| ENST00000394217.6 | hg19 | chr11 | 65,360,326 | 65,363,467 | 3,142 |
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