Hspd1 - heat shock protein family D (Hsp60) member 1 Gene
Also Known as Hsp60; Hspd1-30p
Species: Rattus norvegicus
Summary
Enables modification-dependent protein binding activity. Involved in several processes, including negative regulation of apoptotic process; positive regulation of cytokine production; and response to ischemia. Located in several cellular components, including mitochondrial crista; peroxisomal matrix; and zymogen granule. Used to study Alzheimer's disease and low tension glaucoma. Biomarker of several diseases, including artery disease (multiple); hydrocephalus; hyperglycemia; pulmonary fibrosis; and varicocele. Human ortholog(s) of this gene implicated in artery disease (multiple); autistic disorder; glucose intolerance; hereditary spastic paraplegia (multiple); and hypomyelinating leukodystrophy 4. Orthologous to human HSPD1 (heat shock protein family D (Hsp60) member 1). [provided by Alliance of Genome Resources, Apr 2022]
Hspd1 Products (1)
| mRNA | Protein | Name |
|---|---|---|
| NM_022229.2 | NP_071565.2 | 60 kDa heat shock protein, mitochondrial |
| Protein Preferred Names | Protein Names | |
|---|---|---|
|
60 kDa heat shock protein, mitochondrial |
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