FA18A Rabbit Polyclonal Antibody, 50ul Shaker&Mixing The product of NFATC3

The product of NFATC3

Defects in the encoded protein can lead to early onset autosomal recessive muscular dystrophy| in particular limb-girdle muscular dystrophy| type 2C (LGMD2C)

EMR4P may represent a transcribed pseudogene

PTM:Phosphorylated on tyrosine

The protein encoded by this gene is a gelatinase A

FA18A Rabbit Polyclonal Antibody, 50ul Shaker&Mixing The product of NFATC3This gene encodes a membrane protein associated with the Golgi apparatus which plays a crucial role in intracellular vesicular transport. The encoded protein is likely associated with the late (trans) Golgi compartments which are involved in the delivery of secretory and membrane proteins to the endosome lysosome or the plasma membrane. Alternative splicing results in multiple transcript variants.