HSPA13 (heat shock protein family A (Hsp70) member 13)
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Gene
Gene information from NCBI Gene database.
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| Entrez ID | 6782 |
| Gene name | Heat shock protein family A (Hsp70) member 13 |
| Gene symbol | HSPA13 |
| Synonyms (NCBI Gene) |
STCH
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| Chromosome | 21 |
| Chromosome location | 21q11.2 |
| Summary | The protein encoded by this gene is a member of the heat shock protein 70 family and is found associated with microsomes. Members of this protein family play a role in the processing of cytosolic and secretory proteins, as well as in the removal of denatu |
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miRNA
miRNA information provided by mirtarbase database.
428
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Gene ontology (GO)
Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
16
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Other IDs
Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
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Protein
Protein information from UniProt database.
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UniProt ID
Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
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P48723 | |||||||||||||||
| Protein name | Heat shock 70 kDa protein 13 (Heat shock protein family A member 13) (Microsomal stress-70 protein ATPase core) (Stress-70 protein chaperone microsome-associated 60 kDa protein) | |||||||||||||||
| Protein function | Has peptide-independent ATPase activity. | |||||||||||||||
| Family and domains |
Pfam
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| Tissue specificity | TISSUE SPECIFICITY: Constitutively expressed in all tissues. | |||||||||||||||
| Sequence | ||||||||||||||||
| Sequence length | 471 | |||||||||||||||
| Interactions | View interactions | |||||||||||||||
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Pathways
Pathway information has different metabolic/signaling pathways associated with genes.
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Associated diseases
Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
1
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Evidence Score:
★☆☆☆☆ Gene-disease association found in Text Mining only
★★☆☆☆ Found in Text Mining and Unknown/Other Associations
★★★☆☆ Reported in Unknown/Other Associations across ≥2 Sources
★★★★☆ ClinVar: Pathogenic/Likely Pathogenic (<5 Variants)
★★★★★ ClinVar: Pathogenic/Likely Pathogenic (≥5 Variants)
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