Hello,
I am pretty new to using this database, but I was recently trying to analyze CRISPRGeneeffect of certain paralog proteins that are present either on X or Y chromosomes. XX individuals would have two copies of X version (if it skips inactivation) but one copy each of X and Y proteins. When knocking out a gene that’s present on both X and Y chromosomes, does the screens have different guides to X and Y genes or if it’s the same. Trying to understand if there are any differences in cancer vulnerabilities dependent on X, Y paralogs and their potential differences between male and female cell lines