PHOX2B est un gène codé par le symbole PHOX2B. Communément appelé aussi: Paired mesoderm homeobox protein 2B; Neuroblastoma Phox; NBPhox homeodomain protein; Paired-like homeobox 2B; PMX2B. PHOX2B a une masse de 31.62kDa, une longueur d'acide aminé de 314, et est impliqué dans les maladies: Congenital central hypoventilation syndrome; Neuroblastoma 2.
Nous proposons 7 des anticorps contre PHOX2B, élevé dans Lapin, qui sont appropriés pour le WB et IHC avec des échantillons dérivés de Humain, Souris et Rat.
Informations sur les Gènes et les Protéines
Résumé UniProt
Involved in the development of several major noradrenergic neuron populations, including the locus coeruleus. Transcription factor which could determine a neurotransmitter phenotype in vertebrates. Enhances second-messenger-mediated activation of the dopamine beta-hydrolase and c-fos promoters, and of several enhancers including cAMP-response element and serum-response element.
Résumé Entrez
The DNA-associated protein encoded by this gene is a member of the paired family of homeobox proteins localized to the nucleus. The protein functions as a transcription factor involved in the development of several major noradrenergic neuron populations and the determination of neurotransmitter phenotype. The gene product is linked to enhancement of second messenger-mediated activation of the dopamine beta-hydroylase, c-fos promoters and several enhancers, including cyclic amp-response element and serum-response element. Expansion of a 20 amino acid polyalanine tract in this protein by 5-13 aa has been associated with congenital central hypoventilation syndrome.
Spécificité tissulaire
Expressed in neuroblastoma, brain and adrenal gland.
Implication dans la maladie
Congenital central hypoventilation syndrome: Rare disorder characterized by abnormal control of respiration in the absence of neuromuscular or lung disease, or an identifiable brain stem lesion. A deficiency in autonomic control of respiration results in inadequate or negligible ventilatory and arousal responses to hypercapnia and hypoxemia.
Neuroblastoma 2: A common neoplasm of early childhood arising from embryonic cells that form the primitive neural crest and give rise to the adrenal medulla and the sympathetic nervous system.
Similitudes de séquence
Belongs to the paired homeobox family.
Localisation cellulaire
Nucleus.