TBC1D3A/B/C Polyclonal Antibody, 100ul CellSafe™ Mutations in ELOVL5 have been

Mutations in ELOVL5 have been associated with spinocerebellar ataxia-38 (SCA38)

This gene is partially responsible for IL1-induced upregulation of the transcription factor NF-kappa B

This gene encodes a member of the eyes absent (EYA) family of proteins

moderately expressed in heart and skeletal muscle and at low levels in lung

TBC1D3A/B/C Polyclonal Antibody, 100ul CellSafe™ Mutations in ELOVL5 have beenTBC1D3 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.