CSX1 / NKX2-5 polyclonal, anti-human, mouse, rat

Background:
This gene encodes a homeobox-containing transcription factor. This transcription factor functions in heart formation and development. Mutations in this gene cause atrial septal defect with atrioventricular conduction defect, and also tetralogy of Fallot, which are both heart malformation diseases. Mutations in this gene can also cause congenital hypothyroidism non-goitrous type 5, a non-autoimmune condition. Alternative splicing results in multiple transcript variants.

Other Names:
Homeobox protein Nkx-2.5, Cardiac-specific homeobox, Homeobox protein CSX, Homeobox protein NK-2 homolog E, NKX2-5, CSX, NKX2.5, NKX2E

Antigen Types:
Synthetic Peptide

Gene Name:
NKX2-5
Gene ID:
1482
Primary Accession: P52952
Other Accession: NP_001159648;1482;18091 (mouse); 114109 (rat);