SLC6A15 Polyclonal Antibody, 50ul Fluorescent Staining Diseases associated with CLPTM1 include

Diseases associated with CLPTM1 include cleft lip

The encoded protein may form a heterodimer with another potassium channel protein and may be responsible for the potassium buffering action of glial cells in the brain

It is essential for the development of functional skeletal muscle

a change in platelet shape

q34) with BRD3 which produces a BRD3-NUT fusion protein

SLC6A15 Polyclonal Antibody, 50ul Fluorescent Staining Diseases associated with CLPTM1 includeSLC6A15 (solute carrier family 6 member 15) encodes a member of the solute carrier family 6 protein family which transports neutral amino acids. The encoded protein is thought to play a role in neuronal amino acid transport (PMID: 16185194) and may be associated with major depression (PMID: 21521612). Multiple transcript variants encoding different isoforms have been found for SLC6A15.