ATP4B ATPase H+/K+ transporting subunit beta
Information
- Symbol
- ATP4B
- Type
- protein-coding
- Description
- ATPase H+/K+ transporting subunit beta
- Entrez Gene ID
- 496
- Genome
- hg19
- Position
- chr13:114,303,119-114,312,513
- Genome
- hg38
- Position
- chr13:113,648,804-113,658,198
- MIM
- 137217 OMIM
- HGNC
- HGNC:820 HGNC
- Ensembl
- ENSG00000186009 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Likely benign | 0 | 6 |
Uncertain significance | 0 | 38 |
Ranking
ClinVar | |
---|---|
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0 |
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0 |
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0 |
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44 |
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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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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 |
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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 | ATP6B |
MIM | 137217 OMIM |
HGNC | HGNC:820 HGNC |
Ensembl | ENSG00000186009 Ensembl |
AllianceGenome | HGNC:820 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000335288.5 | hg38 | chr13 | 113,648,804 | 113,658,198 | 9,395 |
ENST00000335288.5 | hg19 | chr13 | 114,303,119 | 114,312,513 | 9,395 |
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