FSHD region gene 2 family member M, pseudogene (FRG2MP)

FSHD region gene 2 family member M, pseudogene (FRG2MP) is classified as a pseudogene, meaning it is a segment of DNA that resembles a protein-coding gene but is generally nonfunctional and not transcribed into an active protein[5][3]. It is distinct from protein-coding members of the FSHD region gene family, such as FRG2, and does not participate in known biological processes, disease mechanisms, or therapeutic interventions[5][1]. Pseudogenes like FRG2MP are often remnants of evolutionary gene duplication events and are typically not involved in cellular signaling, metabolism, or disease pathogenesis. If you need structured variant or protein-coding target information, refer to FRG2 (FSHD region gene 2), which is related to muscular dystrophy but is distinct from FRG2MP[1].

Other names

FRG2MPFSHD region gene 2 family member M, pseudogene