HSPB2 heat shock protein family B (small) member 2
Information
- Symbol
- HSPB2
- Type
- protein-coding
- Description
- heat shock protein family B (small) member 2
- Entrez Gene ID
- 3316
- Genome
- hg19
- Position
- chr11:111,783,458-111,784,817
- Genome
- hg38
- Position
- chr11:111,912,734-111,914,093
- MIM
- 602179 OMIM
- HGNC
- HGNC:5247 HGNC
- Ensembl
- ENSG00000170276 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 0 | 2 |
Uncertain significance | 0 | 16 |
Ranking
ClinVar | |
---|---|
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0 |
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0 |
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0 |
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18 |
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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 |
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 |
---|---|
SYNONYM | HSP27 |
SYNONYM | Hs.78846 |
SYNONYM | LOH11CR1K |
SYNONYM | MKBP |
MIM | 602179 OMIM |
HGNC | HGNC:5247 HGNC |
Ensembl | ENSG00000170276 Ensembl |
AllianceGenome | HGNC:5247 |
Descrption | Source | Links |
---|
ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000304298.4 | hg38 | chr11 | 111,912,734 | 111,914,093 | 1,360 |
ENST00000304298.4 | hg19 | chr11 | 111,783,458 | 111,784,817 | 1,360 |
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