disease:Defects in AIP are a cause of ACTH-secreting pituitary adenoma [MIM:219090]; also known as pituitary Cushing disease. Cushing disease is a condition associated with increased blood cortisol resulting from adrenocorticotropic hormone (ACTH)-producing pituitary tumors that are resistant to glucocorticoid negative feedback.,disease:Defects in AIP are a cause of familial isolated pituitary adenoma (FIPA) [MIM:102200].,disease:Defects in AIP are a cause of growth hormone-secreting pituitary adenoma [MIM:102200]; also known as familial isolated somatotropinomas (FIS) or isolated familial somatotropinoma (IFS) or familial somatotrophinoma or acromegaly due to pituitary adenoma.,disease:Defects in AIP are a cause of pituitary adenoma predisposition (PAP) [MIM:102200].,function:Cellular negative regulator of the hepatitis B virus (HBV) X protein.,function:May play a positive role in AHR-mediated (aromatic hydrocarbon receptor) signaling, possibly by influencing its receptivity for ligand and/or its nuclear targeting.,similarity:Contains 1 PPIase FKBP-type domain.,similarity:Contains 2 TPR repeats.,tissue specificity:Widely expressed. Higher levels seen in the heart, placenta and skeletal muscle. Not expressed in the liver.,
Cytoplasm.
Widely expressed. Higher levels seen in the heart, placenta and skeletal muscle. Not expressed in the liver.