Vasopressin ist ein Gen, das durch das Symbol AVP kodiert wird. Es ist auch bekannt als: Vasopressin-neurophysin 2-copeptin; AVP-NPII; AVP; ARVP; VP. Vasopressin hat eine Masse von 17.33kDa, eine Aminosäurelänge von 164, und ist an Diabetes insipidus, neurohypophyseal beteiligt.
Wir bieten 13 Vasopressin ELISA-Kits zum qualitativen oder quantitativen Nachweis von Vasopressin von Human, Maus, Ratte, Rind, Schwein, Schaf und Hund proben.
Gen- und Proteininformationen
UniProt Zusammenfassung
Neurophysin 2 specifically binds vasopressin.
Entrez Zusammenfassung
This gene encodes a member of the vasopressin/oxytocin family and preproprotein that is proteolytically processed to generate multiple protein products. These products include the neuropeptide hormone arginine vasopressin, and two other peptides, neurophysin 2 and copeptin. Arginine vasopressin is a posterior pituitary hormone that is synthesized in the supraoptic nucleus and paraventricular nucleus of the hypothalamus. Along with its carrier protein, neurophysin 2, it is packaged into neurosecretory vesicles and transported axonally to the nerve endings in the neurohypophysis where it is either stored or secreted into the bloodstream. The precursor is thought to be activated while it is being transported along the axon to the posterior pituitary. Arginine vasopressin acts as a growth factor by enhancing pH regulation through acid-base transport systems. It has a direct antidiuretic action on the kidney, and also causes vasoconstriction of the peripheral vessels. This hormone can contract smooth muscle during parturition and lactation. It is also involved in cognition, tolerance, adaptation and complex sexual and maternal behaviour, as well as in the regulation of water excretion and cardiovascular functions. Mutations in this gene cause autosomal dominant neurohypophyseal diabetes insipidus (ADNDI). This gene is present in a gene cluster with the related gene oxytocin on chromosome 20.
Rolle bei Krankheiten
Diabetes insipidus, neurohypophyseal: A disease characterized by persistent thirst, polydipsia and polyuria. Affected individuals are apparently normal at birth, but characteristically develop symptoms of vasopressin deficiency during childhood.
Sequenzähnlichkeiten
Belongs to the vasopressin/oxytocin family.