KCNG4 potassium voltage-gated channel modifier subfamily G member 4
Information
- Symbol
- KCNG4
- Type
- protein-coding
- Description
- potassium voltage-gated channel modifier subfamily G member 4
- Entrez Gene ID
- 93107
- Genome
- hg19
- Position
- chr16:84,252,263-84,273,618
- Genome
- hg38
- Position
- chr16:84,218,657-84,240,012
- MIM
- 607603 OMIM
- HGNC
- HGNC:19697 HGNC
- Ensembl
- ENSG00000168418 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 0 | 10 |
Likely benign | 0 | 4 |
Uncertain significance | 0 | 92 |
Ranking
ClinVar | |
---|---|
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0 |
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0 |
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0 |
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106 |
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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
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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 |
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Entry | Origin | Type | Annotation | Entry | Origin | Annotation |
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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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Name | MGeND | Type | Genome | Gene symbol | Chromosome | Genomic start | Genomic stop | Strand | Ref | Alt | ClinVar | Origin | Entry | CIViC evidence | DisGeNET entry | |||
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Entry | Origin | Type | Annotation |
Type | ID |
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SYNONYM | KV6.3 |
SYNONYM | KV6.4 |
MIM | 607603 OMIM |
HGNC | HGNC:19697 HGNC |
Ensembl | ENSG00000168418 Ensembl |
AllianceGenome | HGNC:19697 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000568181.1 | hg38 | chr16 | 84,235,408 | 84,239,750 | 4,343 |
ENST00000308251.6 | hg38 | chr16 | 84,218,657 | 84,240,012 | 21,356 |
ENST00000308251.6 | hg19 | chr16 | 84,252,263 | 84,273,618 | 21,356 |
ENST00000568181.1 | hg19 | chr16 | 84,269,014 | 84,273,356 | 4,343 |
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