TBC1D3A/B/C Polyclonal Antibody, 50ul Recombinant Protein Expression Defects in this gene are

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

The family members modulate the activity of GATA family proteins

RCF: 21380×g

% identical to mouse Mekk3

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

TBC1D3A/B/C Polyclonal Antibody, 50ul Recombinant Protein Expression Defects in this gene areTBC1D3 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.