KCNK17 potassium two pore domain channel subfamily K member 17
Information
- Symbol
- KCNK17
- Type
- protein-coding
- Description
- potassium two pore domain channel subfamily K member 17
- Entrez Gene ID
- 89822
- Genome
- hg19
- Position
- chr6:39,266,777-39,282,195
- Genome
- hg38
- Position
- chr6:39,299,001-39,314,419
- MIM
- 607370 OMIM
- HGNC
- HGNC:14465 HGNC
- Ensembl
- ENSG00000124780 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Likely pathogenic | 0 | 2 |
Benign | 0 | 4 |
Likely benign | 0 | 8 |
Uncertain significance | 0 | 42 |
Ranking
ClinVar | |
---|---|
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0 |
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0 |
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0 |
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50 |
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6 |
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 | |||||
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Entry | Origin | Type | Annotation | Entry | Origin | Annotation |
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Target data | : |
MGeND data only
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Name | MGeND | Type | Genome | Size | Chromosome | Start | Stop | Ref | Alt | ClinVar | Origin | Entry | CIViC evidence | DisGeNET entry | |||
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Entry | Origin | Type | Annotation |
Search Word
Target data | : |
MGeND data only
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Category | : |
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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 | K2p17.1 |
SYNONYM | TALK-2 |
SYNONYM | TALK2 |
SYNONYM | TASK-4 |
SYNONYM | TASK4 |
MIM | 607370 OMIM |
HGNC | HGNC:14465 HGNC |
Ensembl | ENSG00000124780 Ensembl |
AllianceGenome | HGNC:14465 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000453413.2 | hg38 | chr6 | 39,299,012 | 39,314,461 | 15,450 |
ENST00000373231.9 | hg38 | chr6 | 39,299,001 | 39,314,419 | 15,419 |
ENST00000373231.9 | hg19 | chr6 | 39,266,777 | 39,282,195 | 15,419 |
ENST00000453413.2 | hg19 | chr6 | 39,266,788 | 39,282,237 | 15,450 |
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