HSPA9 gene

heat shock protein family A (Hsp70) member 9

The information on this page was automatically extracted from online scientific databases.

From NCBI Gene:

This gene encodes a member of the heat shock protein 70 gene family. The encoded protein is primarily localized to the mitochondria but is also found in the endoplasmic reticulum, plasma membrane and cytoplasmic vesicles. This protein is a heat-shock cognate protein. This protein plays a role in cell proliferation, stress response and maintenance of the mitochondria. A pseudogene of this gene is found on chromosome 2.[provided by RefSeq, May 2010]

From UniProt:

Chaperone protein which plays an important role in mitochondrial iron-sulfur cluster (ISC) biogenesis. Interacts with and stabilizes ISC cluster assembly proteins FXN, NFU1, NFS1 and ISCU (PubMed:26702583). Regulates erythropoiesis via stabilization of ISC assembly (PubMed:21123823, PubMed:26702583). May play a role in the control of cell proliferation and cellular aging (By similarity).

From NCBI Gene:

  • Even-plus syndrome
  • Anemia, sideroblastic, 4

From UniProt:

Even-plus syndrome (EVPLS): An autosomal recessive syndrome characterized by epiphyseal and vertebral dysplasia, prenatal-onset short stature, a distinct craniofacial phenotype with microtia, a flat facial profile with flat nose and triangular nares, cardiac malformations, and additional findings such as anal atresia, hypodontia, aplasia cutis, and others. [MIM:616854]

Anemia, sideroblastic, 4 (SIDBA4): A form of sideroblastic anemia, a bone marrow disorder defined by the presence of pathologic iron deposits in erythroblast mitochondria. Sideroblastic anemia is characterized by anemia of varying severity, hypochromic peripheral erythrocytes, systemic iron overload secondary to chronic ineffective erythropoiesis, and the presence of bone marrow ringed sideroblasts. Sideroblasts are characterized by iron-loaded mitochondria clustered around the nucleus. SIDBA4 has been reported to be inherited as an autosomal recessive disease, with a pseudodominant pattern of inheritance in some families. [MIM:182170]

Cytogenetic Location: 5q31.2, which is the long (q) arm of chromosome 5 at position 31.2

Molecular Location: base pairs 138,553,756 to 138,575,401 on chromosome 5 (Homo sapiens Updated Annotation Release 109.20200522, GRCh38.p13) (NCBI)

Cytogenetic Location: 5q31.2, which is the long (q) arm of chromosome 5 at position 31.2
  • CRP40
  • CSA
  • GRP-75
  • GRP75
  • HEL-S-124m
  • HSPA9B
  • MOT
  • MOT2
  • MTHSP75
  • PBP74
  • SAAN
  • SIDBA4