OAT Polyclonal Antibody, 100ul DNA Fragments PSCD family members have identical

PSCD family members have identical structural organization that consists of an N-terminal coiled-coil motif

GO annotations related to this gene include ligase activity and ubiquitin-protein transferase activity

Defects in this gene cause autosomal dominant spinocerebellar ataxia 12 (SCA12)

Among its related pathways are mRNA Splicing - Major Pathway

A small fraction of the human population has been found to harbor an intact allele

OAT Polyclonal Antibody, 100ul DNA Fragments PSCD family members have identicalOAT encodes the mitochondrial enzyme ornithine aminotransferase, which is a key enzyme in the pathway that converts arginine and ornithine into the major excitatory and inhibitory neurotransmitters glutamate and GABA. Mutations that result in a deficiency of this enzyme cause the autosomal recessive eye disease Gyrate Atrophy. Alternatively spliced transcript variants encoding different isoforms have been described. Related pseudogenes have been