Synphilin-1 Polyclonal Antibody, 50ul Rotator Although there is no evidence

Although there is no evidence of transcription from this pseudogene

This gene is a member of the matrix metalloproteinase (MMP) gene family

An important paralog of this gene is ANO5

Defects in this gene are a cause of Fukuyama-type congenital muscular dystrophy (FCMD)

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Synphilin-1 Polyclonal Antibody, 50ul Rotator Although there is no evidenceSNCAIP encodes Synphilin 1 containing several protein protein interaction domains, including ankyrin like repeats, a coiled coil domain, and an ATP GTP binding motif. The synphilin 1 interacts with alpha synuclein in neuronal tissue and may play a role in the formation of cytoplasmic inclusions and neurodegeneration. A mutation in this gene has been associated with Parkinson's disease. Alternative splicing results in multiple transcript variants.