KCNJ9 potassium inwardly rectifying channel subfamily J member 9
Information
- Symbol
- KCNJ9
- Type
- protein-coding
- Description
- potassium inwardly rectifying channel subfamily J member 9
- Entrez Gene ID
- 3765
- Genome
- hg19
- Position
- chr1:160,051,328-160,060,353
- Genome
- hg38
- Position
- chr1:160,081,538-160,090,563
- MIM
- 600932 OMIM
- HGNC
- HGNC:6270 HGNC
- Ensembl
- ENSG00000162728 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Uncertain significance | 0 | 24 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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24 |
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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
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 |
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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 |
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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 | GIRK3 |
SYNONYM | KIR3.3 |
MIM | 600932 OMIM |
HGNC | HGNC:6270 HGNC |
Ensembl | ENSG00000162728 Ensembl |
AllianceGenome | HGNC:6270 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000368088.4 | hg38 | chr1 | 160,081,538 | 160,090,563 | 9,026 |
ENST00000368088.4 | hg19 | chr1 | 160,051,328 | 160,060,353 | 9,026 |
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