2. Gene
  3. HSPA13 - heat shock protein family A (Hsp70) member 13 Gene

HSPA13 - heat shock protein family A (Hsp70) member 13 Gene

  • Gene
  • Protein
  • Disease
  • Agent
  • Ortholog
Homo sapiens

Also known as STCH

Gene ID: 6782 | Gene type: protein coding

About HSPA13

Cytogenetic location: 21q11.2 Genomic coordinates (GRCh38): 21:14,371,115-14,383,146 (from NCBI)

This gene has 2 transcripts (splice variants), 205 orthologues and 13 paralogues. Ubiquitous expression in brain (RPKM 23.3), thyroid (RPKM 21.7) and 25 other tissues.

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 denatured or incorrectly-folded proteins. The encoded protein contains an ATPase domain and has been shown to associate with a ubiquitin-like protein. [provided by RefSeq, Jul 2008]

HSPA13 Products(1)

mRNA Protein Name
NM_006948.5 NP_008879.3 heat shock 70 kDa protein 13 precursor

HSPA13 Protein Structure

HSP70

HSP70: Hsp70 protein (33 - 317)

HSP70

HSP70: Hsp70 protein (358 - 450)

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  • 471 a.a.
Protein Preferred Names Protein Names

heat shock 70 kDa protein 13

heat shock protein 70kDa family, member 13

Related Diseases

Diseases Alias
Bartter Syndrome, Type 1, Antenatal

Hyperprostaglandin E Syndrome 1

Bartter Disease Type 1

BARTS1

Bartter Syndrome, Type 1

Bartter Syndrome Type 1

Hypokalemic Alkalosis With Hypercalciuria Antenatal 1

Hypokalemic Alkalosis With Hypercalciuria 1, Antenatal

Bartter Syndrome Type 1 Antenatal

Hypokalemic Alkalosis With Hypercalciuria 1 Antenatal

Bartter Syndrome Antenatal Type 1

Antenatal Bartter Syndrome Type 1

Bartter Syndrome Type I

Bartter Syndrome 1, Antenatal

Abs1

Antenatal Bartter Syndrome 1

Bs1

Bartter Syndrome, Antenatal Type 1

Antley-Bixler Syndrome With Genital Anomalies And Disordered Steroidogenesis
Deafness, Autosomal Dominant 28

DFNA28

Autosomal Dominant Nonsyndromic Deafness 28

Autosomal Dominant Deafness 28

Deafness, Autosomal Dominant, 28

Non-Syndromic Neurosensory Deafness Autosomal Dominant Type 28

Non-Syndromic Sensorineural Deafness Autosomal Dominant Type 28

Deafness, Autosomal Dominant, Type 28
Diseases Alias
Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Related Agents

Pre-clinical Phase
Bioactive Molecules (1)
Cat. No. Product Name Effect
Purity Rare Diseases
HY-RS06422 HSPA13 Human Pre-designed siRNA Set A / Unkown

Orthologs Information

Species Symbol Source ID
Felis catus HSPA13 VGNC VGNC:102758
Bos taurus HSPA13 VGNC VGNC:53581
Macaca mulatta HSPA13 VGNC VGNC:81327
Rattus norvegicus HSPA13 RGD RGD:3775
Mus musculus HSPA13 MGD MGI:1309463
Canis familiaris HSPA13 VGNC VGNC:53026