Probable DNA helicase; involved in sister-chromatid cohesion and genome integrity and interstrand cross-link repair; interacts with ECO1 and CTF18; mutants are defective in silencing, rDNA recombination, aging and the heat shock response; FANCJ-like helicase family member; mutations in the human homolog, DDX11/ChLR1, cause Warsaw breakage syndrome [Source:SGD;Acc:S000005929]

CTF1, LPA9, MCM12

Chromosome XVI: 539,385-541,970 forward strand.

R64-1-1:BK006949.2

This gene has 1 transcript (splice variant), 371 orthologues and 1 paralogue.

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