ISCU Chromosome 12

Iron-sulfur cluster assembly enzyme
4 variants 4 Health Risk

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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
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
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