M1IP1 Polyclonal Antibody, 20ul Cell Biology Mutations in CCND2 are associated

Mutations in CCND2 are associated with megalencephaly-polymicrogyria-polydactyly-hydrocephalus syndrome 3 (MPPH3)

RNA-binding protein that plays a role in the regulation of alternative splicing and influences mRNA splice site selection and exon inclusion

Required for homologous recombination repair (HRR) and resistance to mitomycin C (MMC)

The protein encoded by this gene is a cytokine structurally related to interleukin 10 (IL10)

M1IP1 Polyclonal Antibody, 20ul Cell Biology Mutations in CCND2 are associatedIt is uncertain whether Met 1 or Met 2 is the initiator.,Involved in stabilization of microtubules.,Belongs to the SPOT14 family.,subcellular location: Associated with microtubules.,