C14orf105
c14orf105, also known as chromosome 14 open reading frame 105, is a gene that encodes a protein of unknown function. This protein is highly conserved across species, suggesting its critical role in cellular processes. However, the exact mechanisms by which c14orf105 exerts its effects are still being actively researched.
Intriguingly, mutations in the c14orf105 gene have been linked to a spectrum of human diseases, including:
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Approximately 1 in 500 individuals are estimated to carry a mutation in the c14orf105 gene. However, the phenotypic consequences of these mutations vary widely, highlighting the complex nature of gene-environment interactions in disease development.