PLOD3 Chromosome 7

Procollagen-lysine,2-oxoglutarate 5-dioxygenase 3
51 variants 51 Health Risk

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What This Gene Does
The protein encoded by this gene is a membrane-bound homodimeric enzyme that is localized to the cisternae of the rough endoplasmic reticulum. The enzyme (cofactors iron and ascorbate) catalyzes the hydroxylation of lysyl residues in collagen-like peptides. The resultant hydroxylysyl groups are attachment sites for carbohydrates in collagen and thus are critical for the stability of intermolecular crosslinks. Some patients with Ehlers-Danlos syndrome type VIB have deficiencies in lysyl hydroxylase activity. [provided by RefSeq, Jul 2008]
Gene Info
Gene Group
Procollagen-lysine,2-oxoglutarate 5-dioxygenase family
Locus Type
gene with protein product
Location
7q22.1
Ensembl
ENSG00000106397
Associated Conditions (14)
Inborn genetic diseases
Acute myeloid leukemia
Clear cell carcinoma of kidney
Gastric cancer
Bone fragility with contractures
arterial rupture
and deafness
Hemorrhage
intracerebral
susceptibility to
PLOD3-related disorder
Lymphoma
Ovarian cancer
Neurodevelopmental delay
Key Variants
All Variants (51)
RSID Category Clinical Significance Conditions
RS748105435 Health Risk Pathogenic/Likely pathogenic Bone fragility with contractures, arterial rupture, and deafness
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