CLPB Chromosome 11
ClpB family mitochondrial disaggregase
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What This Gene Does
This gene belongs to the ATP-ases associated with diverse cellular activities (AAA+) superfamily. Members of this superfamily form ring-shaped homo-hexamers and have highly conserved ATPase domains that are involved in various processes including DNA replication, protein degradation and reactivation of misfolded proteins. All members of this family hydrolyze ATP through their AAA+ domains and use the energy generated through ATP hydrolysis to exert mechanical force on their substrates. In addition to an AAA+ domain, the protein encoded by this gene contains a C-terminal D2 domain, which is characteristic of the AAA+ subfamily of Caseinolytic peptidases to which this protein belongs. It cooperates with Hsp70 in the disaggregation of protein aggregates. Allelic variants of this gene are associated with 3-methylglutaconic aciduria, which causes cataracts and neutropenia. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Apr 2015]
Gene Info
Gene Group
"Ankyrin repeat domain containing|AAA ATPases|Chaperonins"
Locus Type
gene with protein product
Location
11q13.4
Ensembl
ENSG00000162129
Associated Conditions (16)
3-methylglutaconic aciduria
type VIIB
CLPB-related disorder
Inborn genetic diseases
Neutropenia
severe congenital
9
autosomal dominant
Familial cancer of breast
Decreased total neutrophil count
Premature ovarian insufficiency
type VIIA
Microcytic anemia
3-Methylglutaric aciduria
3-Methylglutaconic aciduria
Myeloid maturation arrest
Key Variants
RS116118397
Conflicting classifications of pathogenicity
3-methylglutaconic aciduria, type VIIB, CLPB-related disorder
Health Risk
RS1333709479
Conflicting classifications of pathogenicity
3-methylglutaconic aciduria, type VIIB, 3-methylglutaconic aciduria
Health Risk
RS138797911
Conflicting classifications of pathogenicity
3-methylglutaconic aciduria, type VIIB, 3-methylglutaconic aciduria
Health Risk
RS141970893
Conflicting classifications of pathogenicity
3-methylglutaconic aciduria, type VIIB, Inborn genetic diseases
Health Risk
RS144712077
Conflicting classifications of pathogenicity
3-methylglutaconic aciduria, type VIIB, Inborn genetic diseases
Health Risk
RS146260335
Conflicting classifications of pathogenicity
3-methylglutaconic aciduria, type VIIB, 3-methylglutaconic aciduria
Health Risk
RS150343959
Conflicting classifications of pathogenicity
3-methylglutaconic aciduria, type VIIB, CLPB-related disorder
Health Risk
RS150552809
Conflicting classifications of pathogenicity
3-methylglutaconic aciduria, type VIIB, Inborn genetic diseases
Health Risk
RS150857620
Conflicting classifications of pathogenicity
3-methylglutaconic aciduria, type VIIB, 3-methylglutaconic aciduria
Health Risk
RS1590753221
Conflicting classifications of pathogenicity
3-methylglutaconic aciduria, type VIIB, Neutropenia
Health Risk
RS1590947700
Conflicting classifications of pathogenicity
3-methylglutaconic aciduria, type VIIB, 3-methylglutaconic aciduria
Health Risk
RS200032855
Conflicting classifications of pathogenicity
3-methylglutaconic aciduria, type VIIB, CLPB-related disorder
Health Risk
All Variants (65)
| RSID | Category | Clinical Significance | Conditions |
|---|---|---|---|
| RS748911107 | Health Risk | Pathogenic | 3-methylglutaconic aciduria, type VIIB, 3-methylglutaconic aciduria |
| RS759500860 | Health Risk | Pathogenic | 3-methylglutaconic aciduria, type VIIB, 3-methylglutaconic aciduria |
| RS772512727 | Health Risk | Pathogenic | 3-methylglutaconic aciduria, type VIIB, 3-methylglutaconic aciduria |
| RS774185980 | Health Risk | Pathogenic | 3-methylglutaconic aciduria, type VIIB, 3-methylglutaconic aciduria |
| RS774722200 | Health Risk | Pathogenic | 3-methylglutaconic aciduria, type VIIB, 3-methylglutaconic aciduria |
| RS777202372 | Health Risk | Pathogenic | 3-methylglutaconic aciduria, type VIIB, 3-methylglutaconic aciduria |
| RS786205138 | Health Risk | Pathogenic | 3-methylglutaconic aciduria, type VIIB, 3-methylglutaconic aciduria |
| RS786205139 | Health Risk | Pathogenic | 3-methylglutaconic aciduria, type VIIB, 3-methylglutaconic aciduria |
| RS876657402 | Health Risk | Pathogenic | 3-methylglutaconic aciduria, type VIIB, 3-methylglutaconic aciduria |
| RS144078282 | Health Risk | Pathogenic/Likely pathogenic | 3-methylglutaconic aciduria, type VIIB, Neutropenia |
| RS1466435969 | Health Risk | Pathogenic/Likely pathogenic | — |
| RS1555087619 | Health Risk | Pathogenic/Likely pathogenic | Inborn genetic diseases, 3-methylglutaconic aciduria, type VIIB |
| RS185461628 | Health Risk | Pathogenic/Likely pathogenic | 3-methylglutaconic aciduria, type VIIB, 3-methylglutaconic aciduria |
| RS1951072912 | Health Risk | Pathogenic/Likely pathogenic | 3-methylglutaconic aciduria, type VIIB, 3-methylglutaconic aciduria |
| RS974377052 | Health Risk | Pathogenic/Likely pathogenic | 3-methylglutaconic aciduria, type VIIB, 3-methylglutaconic aciduria |