HSPB7 (heat shock protein family B (small) member 7)
| Gene | |
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Entrez ID
Entrez Gene ID - the GENE ID in NCBI Gene database.
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27129 |
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Gene name
Gene Name - the full gene name approved by the HGNC.
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Heat shock protein family B (small) member 7 |
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Gene symbol
Gene Symbol - the official gene symbol approved by the HGNC.
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HSPB7 |
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Synonyms (NCBI Gene)
Gene synonyms aliases
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cvHSP |
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Chromosome
Chromosome number
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1 |
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Chromosome location
Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
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1p36.13 |
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Summary
Summary of gene provided in NCBI Entrez Gene.
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This gene encodes a small heat shock family B member that can heterodimerize with similar heat shock proteins. Defects in this gene are associated with advanced heart failure. In addition, the encoded protein may be a tumor suppressor in the p53 pathway, |
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miRNA
miRNA information provided by mirtarbase database.
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Gene ontology (GO)
Gene ontology information of associated ontologies with gene provided by GO database.
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Other IDs
Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
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| Protein | |||||||||||
| UniProt ID | Q9UBY9 | ||||||||||
| Protein name | Heat shock protein beta-7 (HspB7) (Cardiovascular heat shock protein) (cvHsp) | ||||||||||
| PDB | 8PA0 , 8RHA | ||||||||||
| Family and domains |
Pfam
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| Tissue specificity | TISSUE SPECIFICITY: Isoform 1 is highly expressed in adult and fetal heart, skeletal muscle, and at a much lower levels in adipose tissue and in aorta. Undetectable in other tissues. Isoform 2 and isoform 3 are poorly detected in heart. | ||||||||||
| Sequence |
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| Sequence length | 170 | ||||||||||
| Interactions | View interactions | ||||||||||
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Associated diseases
Disease associations categorized as Causal (pathogenic variants), Unknown (uncertain genetic evidence), or Text Mining (literature-based associations)
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