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FANCL Polyclonal Antibody, 100ul Diagnostic Probes & Oligos CDH7 is present in a

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FANCL Polyclonal Antibody, 100ul Diagnostic Probes & Oligos CDH7 is present in aThe 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

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Description

CDH7 is present in a gene cluster on chromosome 18

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

GRIN2A encodes a member of the glutamate-gated ion channel protein family

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

Centrosomal protein of 70 kDa is a protein that in humans is encoded by the CEP70 gene

FANCL Polyclonal Antibody, 100ul Diagnostic Probes & Oligos CDH7 is present in aThe 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

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