NCoA-7 Polyclonal Antibody, 20ul Immunoassays Defects in POU4F3 are the

Defects in POU4F3 are the cause of non-syndromic sensorineural deafness autosomal dominant type 15

STK24 encodes Serine/threonine-protein kinase 24 that functions upstream of mitogen-activated protein kinase (MAPK) signaling

HOXA5 is part of the A cluster on chromosome 7 and encodes a DNA-binding transcription factor which may regulate gene expression

Heterogeneous nuclear ribonucleoproteins A2/B1 encoded by HNRNPA2B1 has two repeats of quasi-RRM domains that bind to RNAs

NCoA-7 Polyclonal Antibody, 20ul Immunoassays Defects in POU4F3 are theNCOA7 (Nuclear Receptor Coactivator 7) is a Protein Coding gene. Diseases associated with NCOA7 include brugada syndrome. Among its related pathways are AHR Pathway (Qiagen). GO annotations related to this gene include ligand dependent nuclear receptor transcription coactivator activity and nuclear hormone receptor binding. An important paralog of this gene is TLDC2. nhances the transcriptional activities of several nuclear receptors. Involved in the