SIL1 Rabbit Polyclonal Antibody, 100ul PCR Series Mutations in this gene are

Mutations in this gene are associated with the growth of certain tumors

Mutations in this gene have been associated with pyruvate carboxylase deficiency

|mass spectrometry: PubMed:10233762|online information:CXCL11 entry|Belongs to the intercrine alpha (chemokine CxC) family

3 that encodes transmembrane protein adipocyte-associated 1 expressed in most tissues

SIL1 Rabbit Polyclonal Antibody, 100ul PCR Series Mutations in this gene areThis gene encodes a resident endoplasmic reticulum (ER) N linked glycoprotein with an N terminal ER targeting sequence 2 putative N glycosylation sites and a C terminal ER retention signal. This protein functions as a nucleotide exchange factor for another unfolded protein response protein. Mutations in this gene have been associated with Marinesco Sjogren syndrome. Alternate transcriptional splice variants have been characterized.