FKBP11
Description
The FKBP11 (FKBP prolyl isomerase 11) is a protein-coding gene located on chromosome 12.
FKBP11, also known as peptidyl-prolyl cis-trans isomerase FKBP11, acts as a catalyst to speed up the folding of proteins during their synthesis.
FKBP11 is also known as FKBP19.
Associated Diseases
- nonpapillary renal cell carcinoma
- dacryocystitis-osteopoikilosis syndrome
- melorheostosis
- gnathodiaphyseal dysplasia
- immunodeficiency 75
- 12q14 microdeletion syndrome
- immunodeficiency, common variable, 14
- pyknoachondrogenesis
- neuronal ceroid lipofuscinosis 1
- osteomesopyknosis
- hyper-IgM syndrome type 5
- hyper-IgM syndrome type 3
- IgE responsiveness, atopic
- hyper-IgE recurrent infection syndrome 5, autosomal recessive
- immunodeficiency due to selective anti-polysaccharide antibody deficiency