PYROXD1 Chromosome 12
Pyridine nucleotide-disulphide oxidoreductase domain 1
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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
RS140460108
Conflicting classifications of pathogenicity
Inborn genetic diseases, Myofibrillar myopathy 8, Inborn genetic diseases
Health Risk
RS140536982
Conflicting classifications of pathogenicity
Inborn genetic diseases, Inborn genetic diseases
Health Risk
RS199852910
Conflicting classifications of pathogenicity
Health Risk
RS370239493
Conflicting classifications of pathogenicity
Inborn genetic diseases, Inborn genetic diseases
Health Risk
RS762923417
Conflicting classifications of pathogenicity
Inborn genetic diseases, Inborn genetic diseases
Health Risk
RS1404554956
Likely pathogenic
Health Risk
RS1942824066
Likely pathogenic
Health Risk
RS2540248611
Likely pathogenic
Thyroid cancer, nonmedullary, 1
Health Risk
RS2540258330
Likely pathogenic
Health Risk
RS768153615
Likely pathogenic
Health Risk
RS1057518754
Pathogenic
Myofibrillar myopathy 8, Myofibrillar myopathy 8
Health Risk
RS1057518755
Pathogenic
Myofibrillar myopathy 8, Myofibrillar myopathy 8
Health Risk
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 |