ISCU Chromosome 12
Iron-sulfur cluster assembly enzyme
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What This Gene Does
This gene encodes a component of the iron-sulfur (Fe-S) cluster scaffold. Fe-S clusters are cofactors that play a role in the function of a diverse set of enzymes, including those that regulate metabolism, iron homeostasis, and oxidative stress response. Alternative splicing results in transcript variants encoding different protein isoforms that localize either to the cytosol or to the mitochondrion. Mutations in this gene have been found in patients with hereditary myopathy with lactic acidosis. A disease-associated mutation in an intron may activate a cryptic splice site, resulting in the production of a splice variant encoding a putatively non-functional protein. A pseudogene of this gene is present on chromosome 1. [provided by RefSeq, Feb 2016]
Gene Info
Gene Group
Mitochondrial iron-sulfur assembly components
Locus Type
gene with protein product
Location
12q23.3
Ensembl
ENSG00000136003
Associated Conditions (3)
Inborn genetic diseases
Hereditary myopathy with lactic acidosis due to ISCU deficiency
ISCU-related disorder
Key Variants
RS142514490
Conflicting classifications of pathogenicity
Inborn genetic diseases, Inborn genetic diseases
Health Risk
RS558084375
Conflicting classifications of pathogenicity
Hereditary myopathy with lactic acidosis due to ISCU deficiency, ISCU-related disorder, Hereditary myopathy with lactic acidosis due to ISCU deficiency
Health Risk
RS267607190
Likely pathogenic
Hereditary myopathy with lactic acidosis due to ISCU deficiency, Hereditary myopathy with lactic acidosis due to ISCU deficiency
Health Risk
RS767000507
Pathogenic
Hereditary myopathy with lactic acidosis due to ISCU deficiency, Hereditary myopathy with lactic acidosis due to ISCU deficiency
Health Risk
All Variants (4)
| RSID | Category | Clinical Significance | Conditions |
|---|---|---|---|
| RS142514490 | Health Risk | Conflicting classifications of pathogenicity | Inborn genetic diseases, Inborn genetic diseases |
| RS558084375 | Health Risk | Conflicting classifications of pathogenicity | Hereditary myopathy with lactic acidosis due to ISCU deficiency, ISCU-related disorder, Hereditary myopathy with lactic acidosis due to ISCU deficiency |
| RS267607190 | Health Risk | Likely pathogenic | Hereditary myopathy with lactic acidosis due to ISCU deficiency, Hereditary myopathy with lactic acidosis due to ISCU deficiency |
| RS767000507 | Health Risk | Pathogenic | Hereditary myopathy with lactic acidosis due to ISCU deficiency, Hereditary myopathy with lactic acidosis due to ISCU deficiency |