Ret Polyclonal Antibody, 100ul[BT-AP07761] Enzyme Activity Assays a disease associated with an

a disease associated with an heterogeneous group of cerebellar disorders

Mutations in this gene are associated with spondylometaphyseal dysplasia with cone-rod dystrophy

membrane-bound proteins involved in vesicular fusion and trafficking

Studies of the orthologous gene in rat have shown that the encoded protein selectively modulates spontaneous synaptic-vesicle exocytosis and may also be involved in regulating calcium independent secretion in nonneuronal cells

There is a read-through locus (GeneID: 100526761) that shares sequence identity with this gene and the upstream CCDC169 (GeneID: 728591)

Ret Polyclonal Antibody, 100ul[BT-AP07761] Enzyme Activity Assays a disease associated with anRET (ret proto oncogene), a member of the cadherin superfamily, encodes one of the receptor tyrosine kinases, which are cell surface molecules that transduce signals for cell growth and differentiation. RET plays a crucial role in neural crest development, and it can undergo oncogenic activation in vivo and in vitro by cytogenetic rearrangement. Mutations in RET are associated with the disorders multiple endocrine neoplasia, type IIA, multiple