Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
3336
Gene name Gene Name - the full gene name approved by the HGNC.
Heat shock protein family E (Hsp10) member 1
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
HSPE1
Synonyms (NCBI Gene) Gene synonyms aliases
CPN10, EPF, GROES, HSP10
Chromosome Chromosome number
2
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
2q33.1
Summary Summary of gene provided in NCBI Entrez Gene.
This gene encodes a major heat shock protein which functions as a chaperonin. Its structure consists of a heptameric ring which binds to another heat shock protein in order to form a symmetric, functional heterodimer which enhances protein folding in an A
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT1056772 hsa-miR-1 CLIP-seq
MIRT1056773 hsa-miR-103a CLIP-seq
MIRT1056774 hsa-miR-107 CLIP-seq
MIRT1056775 hsa-miR-1243 CLIP-seq
MIRT1056776 hsa-miR-1270 CLIP-seq
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0001649 Process Osteoblast differentiation HDA 16210410
GO:0003723 Function RNA binding HDA 22658674
GO:0005515 Function Protein binding IPI 9989505, 32296183
GO:0005524 Function ATP binding IEA
GO:0005739 Component Mitochondrion IDA 10205158
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
600141 5269 ENSG00000115541
Protein
UniProt ID P61604
Protein name 10 kDa heat shock protein, mitochondrial (Hsp10) (10 kDa chaperonin) (Chaperonin 10) (CPN10) (Early-pregnancy factor) (EPF) (Heat shock protein family E member 1)
Protein function Co-chaperonin implicated in mitochondrial protein import and macromolecular assembly. Together with Hsp60, facilitates the correct folding of imported proteins. May also prevent misfolding and promote the refolding and proper assembly of unfolde
PDB 4PJ1 , 6HT7 , 6MRC , 6MRD , 8G7N , 8G7O
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00166 Cpn10 8 100 Chaperonin 10 Kd subunit Domain
Sequence
Sequence length 102
Interactions View interactions
Associated diseases Disease information provided by ClinVar, GenCC, and GWAS databases.
Causal
Disease term Disease name dbSNP ID References
Cardiomyopathy Cardiomyopathies, Primary, Cardiomyopathies rs267607003, rs267607002, rs267607004, rs63750743, rs121908333, rs121908334, rs104894655, rs121434420, rs121434421, rs193922674, rs111517471, rs121908987, rs193922384, rs121909374, rs121909377
View all (900 more)
12967636
Unknown
Disease term Disease name Evidence References Source
Schizophrenia Schizophrenia GWAS
Insomnia Insomnia GWAS
Associations from Text Mining
Disease Name Relationship Type References
Abortion Habitual Stimulate 28275270
Adenocarcinoma Associate 27491302
Adenocarcinoma Stimulate 39267762
Adenocarcinoma of Lung Associate 32986659, 38017020
Adenoma Associate 27491302
Alzheimer Disease Associate 26687188
Arthritis Rheumatoid Associate 17457039
Astrocytoma Associate 29028811
Ataxia Telangiectasia Associate 26429916
Carcinogenesis Stimulate 12860287