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Literature summary for 1.6.2.2 extracted from

  • Mota Vieira, L.; Kaplan, J.C.; Kahn, A.; Leroux, A.
    Heterogeneity of the rat NADH-cytochrome-b5-reductase transcripts resulting from multiple alternative first exons (1994), Eur. J. Biochem., 220, 729-737.
    View publication on PubMed

Organism

Organism UniProt Comment Textmining
Homo sapiens
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deficiency leads to 2 different types of recessive congenital methemoglobinemia, in type 1 the soluble enzyme in erythrocytes is affected, in type 2 both soluble and membrane-bound isoforms are affected
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Rattus norvegicus
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enzyme is expressed through the use of at least 4 different promotors
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Source Tissue

Source Tissue Comment Organism Textmining
brain transcripts of L, X and Y mRNAs are detected Rattus norvegicus
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erythrocyte
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Homo sapiens
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erythrocyte transcript of R mRNA is detected Rattus norvegicus
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kidney transcripts of L, X and Y mRNAs are detected Rattus norvegicus
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liver
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Homo sapiens
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liver transcripts of L, X and Y mRNAs are detected Rattus norvegicus
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lung transcripts of L, X and Y mRNAs are detected Rattus norvegicus
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reticulocyte transcripts of L, X, R and Y mRNAs are detected Rattus norvegicus
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