hnRNP DL Polyclonal Antibody, 50ul Funnels Mutations in this gene cause

Mutations in this gene cause syndromic microphthalmia 5 (MCOPS5) and combined pituitary hormone deficiency 6 (CPHD6)

The activity of this receptor is mediated by a G-protein that activate a phosphatidylinositol-calcium second messenger system

A related solute carrier family 11 protein gene is located on chromosome 2

It has a highly restricted target cell specificity acting only on endothelial cells

Two predominant isoforms and a number of minor isoforms are produced by alternatively spliced transcripts

hnRNP DL Polyclonal Antibody, 50ul Funnels Mutations in this gene causeHNRNPDL (heterogeneous nuclear ribonucleoprotein D like) belongs to the subfamily of ubiquitously expressed heterogeneous nuclear ribonucleoproteins (hnRNPs). The hnRNPs are RNA binding proteins and they complex with heterogeneous nuclear RNA (hnRNA). These proteins are associated with pre mRNAs in the nucleus and appear to influence pre mRNA processing and other aspects of mRNA metabolism and transport. While all of the hnRNPs are present in the