HSPB9 heat shock protein family B (small) member 9
Information
- Symbol
- HSPB9
- Type
- protein-coding
- Description
- heat shock protein family B (small) member 9
- Entrez Gene ID
- 94086
- Genome
- hg19
- Position
- chr17:40,274,822-40,275,370
- Genome
- hg38
- Position
- chr17:42,122,804-42,123,352
- MIM
- 608344 OMIM
- HGNC
- HGNC:30589 HGNC
- Ensembl
- ENSG00000260325 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Uncertain significance | 0 | 18 |
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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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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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 | CT51 |
MIM | 608344 OMIM |
HGNC | HGNC:30589 HGNC |
Ensembl | ENSG00000260325 Ensembl |
AllianceGenome | HGNC:30589 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000565659.2 | hg38 | chr17 | 42,122,804 | 42,123,352 | 549 |
ENST00000565659.2 | hg19 | chr17 | 40,274,822 | 40,275,370 | 549 |
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