PYROXD1 Chromosome 12

Pyridine nucleotide-disulphide oxidoreductase domain 1
24 variants 24 Health Risk

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What This Gene Does
This gene encodes a nuclear-cytoplasmic pyridine nucleotide-disulphide reductase (PNDR). PNDRs are flavoproteins that catalyze the pyridine nucleotide-dependent reduction of thiol residues in other proteins. The encoded protein belongs to the class I pyridine nucleotide-disulphide oxidoreductase family but lacks the C-terminal dimerization domain found in other family members and instead has a C-terminal nitrile reductase domain. It localizes to the nucleus and to striated sarcomeric compartments. Naturally occurring mutations in this gene cause early-onset myopathy with internalized nuclei and myofibrillar disorganization. A pseudogene of this gene has been defined on chromosome 11. [provided by RefSeq, Apr 2017]
Gene Info
Gene Group
Flavoproteins
Locus Type
gene with protein product
Location
12p12.1
Ensembl
ENSG00000121350
Associated Conditions (5)
Inborn genetic diseases
Myofibrillar myopathy 8
Thyroid cancer
nonmedullary
1
Key Variants
All Variants (24)
RSID Category Clinical Significance Conditions
RS140460108 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Myofibrillar myopathy 8, Inborn genetic diseases
RS140536982 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS199852910 Health Risk Conflicting classifications of pathogenicity
RS370239493 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS762923417 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS1404554956 Health Risk Likely pathogenic
RS1942824066 Health Risk Likely pathogenic
RS2540248611 Health Risk Likely pathogenic Thyroid cancer, nonmedullary, 1
RS2540258330 Health Risk Likely pathogenic
RS768153615 Health Risk Likely pathogenic
RS1057518754 Health Risk Pathogenic Myofibrillar myopathy 8, Myofibrillar myopathy 8
RS1057518755 Health Risk Pathogenic Myofibrillar myopathy 8, Myofibrillar myopathy 8
RS1399200035 Health Risk Pathogenic
RS1459973740 Health Risk Pathogenic
RS2540234162 Health Risk Pathogenic
RS2540258311 Health Risk Pathogenic
RS2540289128 Health Risk Pathogenic
RS752009313 Health Risk Pathogenic Myofibrillar myopathy 8, Myofibrillar myopathy 8
RS755208949 Health Risk Pathogenic Myofibrillar myopathy 8, Myofibrillar myopathy 8
RS765752811 Health Risk Pathogenic Myofibrillar myopathy 8, Myofibrillar myopathy 8
RS774637488 Health Risk Pathogenic
RS781565158 Health Risk Pathogenic Myofibrillar myopathy 8, Myofibrillar myopathy 8
RS369083786 Health Risk Pathogenic/Likely pathogenic Myofibrillar myopathy 8, Myofibrillar myopathy 8
RS757103085 Health Risk Pathogenic/Likely pathogenic Myofibrillar myopathy 8, Myofibrillar myopathy 8
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