FANCL Polyclonal Antibody, 100ul Diagnostic Probes & Oligos This gene encodes a Na+/H+

This gene encodes a Na+/H+ antiporter that is a member of the solute carrier family 9

Enhances the transcriptional repressor activity of NR1D1 through stabilization of NR1D1 protein levels by preventing its ubiquitination and subsequent degradation (PubMed: 18235501

also known as X-linked recessive Charcot-Marie-Tooth disease-4 (CMTX-4)

it is present in the cartilage extracellular matrix and has a role in the development and homeostasis of cartilage and bone

insulin resistance

FANCL Polyclonal Antibody, 100ul Diagnostic Probes & Oligos This gene encodes a Na+/H+The Fanconi anemia complementation group (FANC) currently includes FANCA, FANCB, FANCC, FANCD1 (also called BRCA2), FANCD2, FANCE, FANCF, FANCG, FANCI, FANCJ (also called BRIP1), FANCL, FANCM and FANCN (also called PALB2). The previously defined group FANCH is the same as FANCA. Fanconi anemia is a genetically heterogeneous recessive disorder characterized by cytogenetic instability, hypersensitivity to DNA crosslinking agents, increased chromosomal