SIL1 Rabbit Polyclonal Antibody, 100ul PCR Series |mass spectrometry: PubMed:10233762|online information:CXCL11 entry|Belongs

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

Defects in this gene are the cause of LIG4 syndrome

This gene encodes the alpha chain of type XIX collagen

Mutations in this gene have been associated with pyruvate carboxylase deficiency

several pseudogenes of this gene have been located

SIL1 Rabbit Polyclonal Antibody, 100ul PCR Series |mass spectrometry: PubMed:10233762|online information:CXCL11 entry|BelongsThis 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.