MFSD8 Polyclonal Antibody, 50ul Cell Biology Mutations in this gene are

Mutations in this gene are associated with cryptorchidism

This protein has been shown to form a stable complex with CDK4 or CDK6

It has been suggested that this gene could be a candidate gene for Cornelia de Lange syndrome

A pseudogene of ACKR4 is found on chromosome 6

MFSD8 Polyclonal Antibody, 50ul Cell Biology Mutations in this gene areThis gene encodes a ubiquitous integral membrane protein that contains a transporter domain and a major facilitator superfamily (MFS) domain. Other members of the major facilitator superfamily transport small solutes through chemiosmotic ion gradients. The substrate transported by this protein is unknown. The protein likely localizes to lysosomal membranes. Mutations in this gene are correlated with a variant form of late infantile onset neuronal