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Chromosome 1 open reading frame 105 (C1orf105) is a protein-coding gene in humans with largely unknown function. It is classified as a \"protein of unknown function\" and includes a domain DUF4548. Little is known about its molecular role; it may be involved in general protein binding. There are some reported associations with rare diseases such as glycosylphosphatidylinositol biosynthesis defect 16 and nonimmune hydrops fetalis, but C1orf105 is not established as a disease gene nor as a therapeutic target. No drugs, biomarkers, or clear clinical roles are currently attributed to it[1][4][7][8].
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