Gene Symbol: NFU1
OMIM: 608100Chromosome location: 2p13.3
Related informations:  
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Phenotype: |    Multiple mitochondrial dysfunctions syndrome 1 |
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Dna Change: |    c.622G>T |
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Protein Change: |    p.Gly208Cys |
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Mutation Type: |    Substitution |
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Mutation Effect: |    Missense |
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Location: |    exon 7 |
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Transcript: |    NM_001002755.2 |
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Population | Ethnic Group | Region | Mutation Frquency | Coalescence Time | Reference |
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France | NA | NA | 1 patient | NA | Nizon M et al., 2014Nizon M, Boutron A, Boddaert N, Slama A, Delpech H, Sardet C, Brassier A, Habarou F, Delahodde A, Correia I, Ottolenghi C, de Lonlay P, . Leukoencephalopathy with cysts and hyperglycinemia may result from NFU1 deficiency.. Mitochondrion. 2014; 0(0): |
Spain | NA | NA | 10 patients / 9 unrelated families | NA | Navarro-Sastre A et al., 2011Navarro-Sastre A, Tort F, Stehling O, Uzarska MA, Arranz JA, Del Toro M, Labayru MT, Landa J, Font A, Garcia-Villoria J, Merinero B, Ugarte M, Gutierrez-Solana LG, Campistol J, Garcia-Cazorla A, Vaquerizo J, Riudor E, Briones P, Elpeleg O, Ribes A, Lill R, . A fatal mitochondrial disease is associated with defective NFU1 function in the maturation of a subset of mitochondrial Fe-S proteins.. Am. J. Hum. Genet.. 2011; 89(5):656-67 |
Spain | NA | NA | 10 patients / 9 unrelated | NA | Navarro-Sastre A et al., 2011Navarro-Sastre A, Tort F, Stehling O, Uzarska MA, Arranz JA, Del Toro M, Labayru MT, Landa J, Font A, Garcia-Villoria J, Merinero B, Ugarte M, Gutierrez-Solana LG, Campistol J, Garcia-Cazorla A, Vaquerizo J, Riudor E, Briones P, Elpeleg O, Ribes A, Lill R, . A fatal mitochondrial disease is associated with defective NFU1 function in the maturation of a subset of mitochondrial Fe-S proteins.. Am. J. Hum. Genet.. 2011; 89(5):656-67 |
References
Navarro-Sastre A, Tort F, Stehling O, Uzarska MA, Arranz JA, Del Toro M, Labayru MT, Landa J, Font A, Garcia-Villoria J, Merinero B, Ugarte M, Gutierrez-Solana LG, Campistol J, Garcia-Cazorla A, Vaquerizo J, Riudor E, Briones P, Elpeleg O, Ribes A, Lill R, A fatal mitochondrial disease is associated with defective NFU1 function in the maturation of a subset of mitochondrial Fe-S proteins.Am. J. Hum. Genet.. 2011; 89(5):656-67
Nizon M, Boutron A, Boddaert N, Slama A, Delpech H, Sardet C, Brassier A, Habarou F, Delahodde A, Correia I, Ottolenghi C, de Lonlay P, Leukoencephalopathy with cysts and hyperglycinemia may result from NFU1 deficiency.Mitochondrion. 2014; 0(0):