The protein encoded by this gene functions together with DNA ligase IV and the DNA-dependent protein kinase in the repair of DNA double-strand breaks. This protein plays a role in both non-homologous end joining and the completion of V(D)J recombination. Mutations in this gene can cause short stature, microcephaly, and endocrine dysfunction (SSMED). Alternative splicing generates several transcript variants.
A synthesized peptide derived from human XRN1, corresponding to a region within N-terminal amino acids.
A synthesized peptide derived from human XRN2, corresponding to a region within N-terminal amino acids.
A synthesized peptide derived from human XRRA1.
A synthesized peptide derived from human XYLB.
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