HSP90B1 heat shock protein 90 beta family member 1
Information
- Symbol
- HSP90B1
- Type
- protein-coding
- Description
- heat shock protein 90 beta family member 1
- Entrez Gene ID
- 7184
- Genome
- hg19
- Position
- chr12:104,324,188-104,341,704
- Genome
- hg38
- Position
- chr12:103,930,410-103,947,926
- MIM
- 191175 OMIM
- HGNC
- HGNC:12028 HGNC
- Ensembl
- ENSG00000166598 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| Benign | 0 | 2 |
| Likely benign | 0 | 2 |
| Uncertain significance | 0 | 50 |
Ranking
| ClinVar | |
|---|---|
 |
0 |
 |
0 |
 |
0 |
 |
54 |
 |
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 |
Prediction | |||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Entry | Origin | Type | Annotation | Entry | Origin | Annotation | |||||||||||
Search Word
| Target data | : |
MGeND data only
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| Filtering | : |
| Name | MGeND | Type | Genome | Size | Chromosome | Start | Stop | Ref | Alt | ClinVar | Origin | Entry | CIViC evidence | DisGeNET entry | |||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Entry | Origin | Type | Annotation | ||||||||||||||
Search Word
| Target data | : |
MGeND data only
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| Category | : |
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| Search word | : | |
| Filtering | : |
| Name | MGeND | Type | Genome | Gene symbol | Chromosome | Genomic start | Genomic stop | Strand | Ref | Alt | ClinVar | Origin | Entry | CIViC evidence | DisGeNET entry | |||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Entry | Origin | Type | Annotation | |||||||||||||||
| Type | ID |
|---|---|
| SYNONYM | ECGP |
| SYNONYM | GP96 |
| SYNONYM | GRP94 |
| SYNONYM | HEL-S-125m |
| SYNONYM | HEL35 |
| SYNONYM | TRA1 |
| MIM | 191175 OMIM |
| HGNC | HGNC:12028 HGNC |
| Ensembl | ENSG00000166598 Ensembl |
| AllianceGenome | HGNC:12028 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000299767.10 | hg38 | chr12 | 103,930,410 | 103,947,926 | 17,517 |
| ENST00000614327.2 | hg38 | chr12 | 103,930,358 | 103,947,858 | 17,501 |
| ENST00000681861.1 | hg38 | chr12 | 103,930,332 | 103,947,695 | 17,364 |
| ENST00000681949.1 | hg38 | chr12 | 103,930,358 | 103,947,912 | 17,555 |
| ENST00000680762.1 | hg38 | chr12 | 103,930,358 | 103,947,379 | 17,022 |
| ENST00000679861.1 | hg38 | chr12 | 103,930,684 | 103,947,922 | 17,239 |
| ENST00000550595.2 | hg38 | chr12 | 103,930,332 | 103,953,931 | 23,600 |
| ENST00000680316.1 | hg38 | chr12 | 103,930,600 | 103,947,922 | 17,323 |
| ENST00000299767.10 | hg19 | chr12 | 104,324,188 | 104,341,704 | 17,517 |
| ENST00000550595.2 | hg19 | chr12 | 104,324,110 | 104,347,709 | 23,600 |
| ENST00000679861.1 | hg19 | chr12 | 104,324,462 | 104,341,700 | 17,239 |
| ENST00000680316.1 | hg19 | chr12 | 104,324,378 | 104,341,700 | 17,323 |
| ENST00000614327.2 | hg19 | chr12 | 104,324,136 | 104,341,636 | 17,501 |
| ENST00000680762.1 | hg19 | chr12 | 104,324,136 | 104,341,157 | 17,022 |
| ENST00000681861.1 | hg19 | chr12 | 104,324,110 | 104,341,473 | 17,364 |
| ENST00000681949.1 | hg19 | chr12 | 104,324,136 | 104,341,690 | 17,555 |
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