TBC1D3A/B/C Polyclonal Antibody, 50ul Recombinant Protein Expression Mutations in this gene have

Mutations in this gene have been associated with primary microcephaly (MCPH4)

The family members modulate the activity of GATA family proteins

such as NAK (TBK1

Defects in this gene are a cause of congenital disorder of glycosylation| type IIp

Alternatively spliced transcript variants that encode different isoforms have been observed for CIDEC

TBC1D3A/B/C Polyclonal Antibody, 50ul Recombinant Protein Expression Mutations in this gene haveTBC1D3 encodes a protein that is similar to TBC1 domain family, member 3. TBC1 domain family member 3 contains a TBC (Tre 2, Bub2p, and Cdc16p) domain, which is found in proteins involved in RAB GTPase signaling and vesicle trafficking. There are multiple copies of this gene located within a cluster of chemokine genes on chromosome 17q.