HSPE1 heat shock protein family E (Hsp10) member 1
Information
- Symbol
- HSPE1
- Type
- protein-coding
- Description
- heat shock protein family E (Hsp10) member 1
- Entrez Gene ID
- 3336
- Genome
- hg19
- Position
- chr2:198,365,103-198,368,173
- Genome
- hg38
- Position
- chr2:197,500,379-197,503,449
- MIM
- 600141 OMIM
- HGNC
- HGNC:5269 HGNC
- Ensembl
- ENSG00000115541 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 0 | 2 |
Likely benign | 0 | 2 |
Uncertain significance | 0 | 6 |
Ranking
ClinVar | |
---|---|
![]() |
0 |
![]() |
0 |
![]() |
0 |
![]() |
8 |
![]() |
2 |
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
|
Category | : |
|
Search word | : | |
Filtering | : |
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
|
Category | : |
|
Search word | : | |
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
|
Category | : |
|
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 | CPN10 |
SYNONYM | EPF |
SYNONYM | GROES |
SYNONYM | HSP10 |
MIM | 600141 OMIM |
HGNC | HGNC:5269 HGNC |
Ensembl | ENSG00000115541 Ensembl |
AllianceGenome | HGNC:5269 |
Descrption | Source | Links |
---|
ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000409729.1 | hg38 | chr2 | 197,500,140 | 197,503,296 | 3,157 |
ENST00000233893.10 | hg38 | chr2 | 197,500,379 | 197,503,449 | 3,071 |
ENST00000409468.1 | hg38 | chr2 | 197,500,379 | 197,503,382 | 3,004 |
ENST00000409729.1 | hg19 | chr2 | 198,364,864 | 198,368,020 | 3,157 |
ENST00000409468.1 | hg19 | chr2 | 198,365,103 | 198,368,106 | 3,004 |
ENST00000233893.10 | hg19 | chr2 | 198,365,103 | 198,368,173 | 3,071 |
Genome browser