ARP-1 Polyclonal Antibody, 100ul Organelle Studies Mutations in ACTA1 cause nemaline

Mutations in ACTA1 cause nemaline myopathy type 3

Alternate splicing resultsi n multiple transcript variants

The protein encoded by this gene is a subunit of the receptor for IL23A/IL23

subcellular location:Found in postsynaptic density of neuronal cells

ARP-1 Polyclonal Antibody, 100ul Organelle Studies Mutations in ACTA1 cause nemalineNR2F2 encodes a member of the steroid thyroid hormone superfamily of nuclear receptors. The encoded protein (nuclear receptor subfamily 2 group F member 2) is a ligand inducible transcription factor that is involved in the regulation of many different genes. Alternate splicing results in multiple transcript variants.