abnormal dosage compensation Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description anomaly in the process of compensating for the two-fold variation in X:autosome chromosome ratios between sexes by a global activation or inactivation of all, or most of, genes on one or both of the X chromosomes (Mammalian Phenotype Ontology, MP_0010381)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0010381
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Genes

5 gene mutations causing the abnormal dosage compensation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
CUL4B cullin 4B
MECP2 methyl CpG binding protein 2
RLIM ring finger protein, LIM domain interacting
TSIX TSIX transcript, XIST antisense RNA
XIST X inactive specific transcript (non-protein coding)