PEX3 Chromosome 6
Peroxisomal biogenesis factor 3
Upload your DNA to see your personal genotypes for variants in PEX3.
What This Gene Does
The product of this gene is involved in peroxisome biosynthesis and integrity. It assembles membrane vesicles before the matrix proteins are translocated. Peroxins (PEXs) are proteins that are essential for the assembly of functional peroxisomes. The peroxisome biogenesis disorders (PBDs) are a group of genetically heterogeneous autosomal recessive, lethal diseases characterized by multiple defects in peroxisome function. The peroxisomal biogenesis disorders are a heterogeneous group with at least 14 complementation groups and with more than 1 phenotype being observed in cases falling into particular complementation groups. Although the clinical features of PBD patients vary, cells from all PBD patients exhibit a defect in the import of one or more classes of peroxisomal matrix proteins into the organelle. Defects in this gene are a cause Zellweger syndrome (ZWS). [provided by RefSeq, Oct 2008]
Gene Info
Gene Group
Peroxins
Locus Type
gene with protein product
Location
6q24.2
Ensembl
ENSG00000034693
Associated Conditions (7)
Peroxisome biogenesis disorder 10B
Peroxisome biogenesis disorder 10A (Zellweger)
Peroxisome biogenesis disorder 1A (Zellweger)
PEX3-related disorder
Inborn genetic diseases
Hepatocellular carcinoma
Peroxisome biogenesis disorder
Key Variants
RS1024883914
Conflicting classifications of pathogenicity
Health Risk
RS1057523689
Conflicting classifications of pathogenicity
Peroxisome biogenesis disorder 10B, Peroxisome biogenesis disorder 10B
Health Risk
RS117247312
Conflicting classifications of pathogenicity
Peroxisome biogenesis disorder 10A (Zellweger), Peroxisome biogenesis disorder 10A (Zellweger)
Health Risk
RS139760270
Conflicting classifications of pathogenicity
Peroxisome biogenesis disorder 10A (Zellweger), Peroxisome biogenesis disorder 10A (Zellweger)
Health Risk
RS1562654527
Conflicting classifications of pathogenicity
Peroxisome biogenesis disorder 1A (Zellweger), Peroxisome biogenesis disorder 1A (Zellweger)
Health Risk
RS199781957
Conflicting classifications of pathogenicity
Peroxisome biogenesis disorder 10A (Zellweger), PEX3-related disorder, Peroxisome biogenesis disorder 10A (Zellweger)
Health Risk
RS200807211
Conflicting classifications of pathogenicity
Peroxisome biogenesis disorder 10A (Zellweger), Peroxisome biogenesis disorder 10A (Zellweger)
Health Risk
RS201718910
Conflicting classifications of pathogenicity
Peroxisome biogenesis disorder 10A (Zellweger), Peroxisome biogenesis disorder 10A (Zellweger)
Health Risk
RS201793456
Conflicting classifications of pathogenicity
Inborn genetic diseases, Inborn genetic diseases
Health Risk
RS367803197
Conflicting classifications of pathogenicity
Peroxisome biogenesis disorder 10A (Zellweger), Peroxisome biogenesis disorder 10A (Zellweger)
Health Risk
RS41285015
Conflicting classifications of pathogenicity
Peroxisome biogenesis disorder 10A (Zellweger), Peroxisome biogenesis disorder 10A (Zellweger)
Health Risk
RS758701470
Conflicting classifications of pathogenicity
Health Risk
All Variants (40)
| RSID | Category | Clinical Significance | Conditions |
|---|---|---|---|
| RS1024883914 | Health Risk | Conflicting classifications of pathogenicity | — |
| RS1057523689 | Health Risk | Conflicting classifications of pathogenicity | Peroxisome biogenesis disorder 10B, Peroxisome biogenesis disorder 10B |
| RS117247312 | Health Risk | Conflicting classifications of pathogenicity | Peroxisome biogenesis disorder 10A (Zellweger), Peroxisome biogenesis disorder 10A (Zellweger) |
| RS139760270 | Health Risk | Conflicting classifications of pathogenicity | Peroxisome biogenesis disorder 10A (Zellweger), Peroxisome biogenesis disorder 10A (Zellweger) |
| RS1562654527 | Health Risk | Conflicting classifications of pathogenicity | Peroxisome biogenesis disorder 1A (Zellweger), Peroxisome biogenesis disorder 1A (Zellweger) |
| RS199781957 | Health Risk | Conflicting classifications of pathogenicity | Peroxisome biogenesis disorder 10A (Zellweger), PEX3-related disorder, Peroxisome biogenesis disorder 10A (Zellweger) |
| RS200807211 | Health Risk | Conflicting classifications of pathogenicity | Peroxisome biogenesis disorder 10A (Zellweger), Peroxisome biogenesis disorder 10A (Zellweger) |
| RS201718910 | Health Risk | Conflicting classifications of pathogenicity | Peroxisome biogenesis disorder 10A (Zellweger), Peroxisome biogenesis disorder 10A (Zellweger) |
| RS201793456 | Health Risk | Conflicting classifications of pathogenicity | Inborn genetic diseases, Inborn genetic diseases |
| RS367803197 | Health Risk | Conflicting classifications of pathogenicity | Peroxisome biogenesis disorder 10A (Zellweger), Peroxisome biogenesis disorder 10A (Zellweger) |
| RS41285015 | Health Risk | Conflicting classifications of pathogenicity | Peroxisome biogenesis disorder 10A (Zellweger), Peroxisome biogenesis disorder 10A (Zellweger) |
| RS758701470 | Health Risk | Conflicting classifications of pathogenicity | — |
| RS769938240 | Health Risk | Conflicting classifications of pathogenicity | PEX3-related disorder, PEX3-related disorder |
| RS774963514 | Health Risk | Conflicting classifications of pathogenicity | Peroxisome biogenesis disorder 10A (Zellweger), Hepatocellular carcinoma, Peroxisome biogenesis disorder 10A (Zellweger) |
| RS1411756701 | Health Risk | Likely pathogenic | Peroxisome biogenesis disorder 10A (Zellweger), Peroxisome biogenesis disorder 10A (Zellweger) |
| RS1473197986 | Health Risk | Likely pathogenic | Peroxisome biogenesis disorder 10A (Zellweger), Peroxisome biogenesis disorder 10A (Zellweger) |
| RS150841396 | Health Risk | Likely pathogenic | Peroxisome biogenesis disorder 10A (Zellweger), Peroxisome biogenesis disorder 10A (Zellweger) |
| RS2537193194 | Health Risk | Likely pathogenic | Peroxisome biogenesis disorder, Peroxisome biogenesis disorder |
| RS2537196651 | Health Risk | Likely pathogenic | — |
| RS2537199055 | Health Risk | Likely pathogenic | Peroxisome biogenesis disorder, Peroxisome biogenesis disorder |
| RS746152064 | Health Risk | Likely pathogenic | — |
| RS756023893 | Health Risk | Likely pathogenic | — |
| RS958074446 | Health Risk | Likely pathogenic | — |
| RS1243154971 | Health Risk | Pathogenic | Peroxisome biogenesis disorder, Peroxisome biogenesis disorder |
| RS147556993 | Health Risk | Pathogenic | — |
| RS1562653663 | Health Risk | Pathogenic | — |
| RS1562654984 | Health Risk | Pathogenic | — |
| RS201179294 | Health Risk | Pathogenic | Peroxisome biogenesis disorder 10B, Peroxisome biogenesis disorder 10B |
| RS2482437364 | Health Risk | Pathogenic | — |
| RS2537182031 | Health Risk | Pathogenic | — |
| RS2537182158 | Health Risk | Pathogenic | — |
| RS2537186945 | Health Risk | Pathogenic | — |
| RS2537196715 | Health Risk | Pathogenic | — |
| RS2537199126 | Health Risk | Pathogenic | — |
| RS267608193 | Health Risk | Pathogenic | Peroxisome biogenesis disorder 10A (Zellweger), Peroxisome biogenesis disorder 1A (Zellweger), Peroxisome biogenesis disorder 10A (Zellweger) |
| RS62641230 | Health Risk | Pathogenic | Peroxisome biogenesis disorder 10A (Zellweger), Peroxisome biogenesis disorder 10A (Zellweger) |
| RS776831462 | Health Risk | Pathogenic | — |
| RS780088661 | Health Risk | Pathogenic | — |
| RS748689554 | Health Risk | Pathogenic/Likely pathogenic | Peroxisome biogenesis disorder 10A (Zellweger), Peroxisome biogenesis disorder 10A (Zellweger) |
| RS752904598 | Health Risk | Pathogenic/Likely pathogenic | PEX3-related disorder, Peroxisome biogenesis disorder 10A (Zellweger), PEX3-related disorder |