KIRR1 Polyclonal Antibody, 50ul In vitro Assessment Defects in this gene cause

Defects in this gene cause complement factor I deficiency

suggesting that

Protein tyrosine phosphatase

Other polypeptides of subunit VIIa are present in both muscle and nonmuscle tissues| and are encoded by different genes

NPHS1 encodes a member of the immunoglobulin family of cell adhesion molecules that functions in the glomerular filtration barrier in the kidney

KIRR1 Polyclonal Antibody, 50ul In vitro Assessment Defects in this gene causeNEPH1 is a member of the nephrin like protein family, which includes NEPH2 (MIM 607761) and NEPH3 (MIM 607762). The cytoplasmic domains of these proteins interact with the C terminus of podocin (NPHS2; MIM 604766), and the genes are expressed in kidney podocytes, cells involved in ensuring size and charge selective ultrafiltration (Sellin et al., 2003