KCNK16 potassium two pore domain channel subfamily K member 16
Information
- Symbol
- KCNK16
- Type
- protein-coding
- Description
- potassium two pore domain channel subfamily K member 16
- Entrez Gene ID
- 83795
- Genome
- hg19
- Position
- chr6:39,282,597-39,290,316
- Genome
- hg38
- Position
- chr6:39,314,821-39,322,540
- MIM
- 607369 OMIM
- HGNC
- HGNC:14464 HGNC
- Ensembl
- ENSG00000095981 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| Likely benign | 0 | 6 |
| Uncertain significance | 0 | 36 |
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 | K2p16.1 |
| SYNONYM | TALK-1 |
| SYNONYM | TALK1 |
| MIM | 607369 OMIM |
| HGNC | HGNC:14464 HGNC |
| Ensembl | ENSG00000095981 Ensembl |
| AllianceGenome | HGNC:14464 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000437525.3 | hg38 | chr6 | 39,316,171 | 39,322,702 | 6,532 |
| ENST00000425054.6 | hg38 | chr6 | 39,314,821 | 39,322,540 | 7,720 |
| ENST00000373227.8 | hg38 | chr6 | 39,315,002 | 39,322,540 | 7,539 |
| ENST00000373229.9 | hg38 | chr6 | 39,314,698 | 39,322,554 | 7,857 |
| ENST00000507712.5 | hg38 | chr6 | 39,314,948 | 39,322,968 | 8,021 |
| ENST00000373229.9 | hg19 | chr6 | 39,282,474 | 39,290,330 | 7,857 |
| ENST00000425054.6 | hg19 | chr6 | 39,282,597 | 39,290,316 | 7,720 |
| ENST00000507712.5 | hg19 | chr6 | 39,282,724 | 39,290,744 | 8,021 |
| ENST00000373227.8 | hg19 | chr6 | 39,282,778 | 39,290,316 | 7,539 |
| ENST00000437525.3 | hg19 | chr6 | 39,283,947 | 39,290,478 | 6,532 |
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