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- Table of Contents
Facts about Inactive peptidyl-prolyl cis-trans isomerase FKBP6.
Acts as a co-chaperone through its interaction with HSP90 and is needed for the piRNA amplification process, the secondary piRNA biogenesis. May be required together with HSP90 in elimination of 16 nucleotide ping-pong by-products from Piwi complexes, possibly facilitating turnover of Piwi complexes (By similarity).
Human | |
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Gene Name: | FKBP6 |
Uniprot: | O75344 |
Entrez: | 8468 |
Belongs to: |
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FKBP6 family |
36 kDa FKBP; EC 5.2.1.8; FK506 binding protein 6, 36kDa; FK506-binding protein 6 (36kD); FK506-binding protein 6; FKBP-36; FKBP36MGC87179; FKBP-6; Immunophilin FKBP36; peptidyl-prolyl cis-trans isomerase FKBP6,36 kDa FK506-binding protein; PPIase FKBP6; PPIase; rotamase
Mass (kDA):
37.214 kDA
Human | |
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Location: | 7q11.23 |
Sequence: | 7; NC_000007.14 (73328154..73358625) |
Detected in all tissues examined, with higher expression in testis, heart, skeletal muscle, liver, and kidney.
Cytoplasm, cytosol. Nucleus. Chromosome. Does not localize to pi-bodies. Localizes to meiotic chromosome cores and regions of homologous chromosome synapsis (By similarity).
PMID: 9782077 by Meng X., et al. A novel human gene FKBP6 is deleted in Williams syndrome.
PMID: 15770126 by Metcalfe K., et al. Autosomal dominant inheritance of Williams-Beuren syndrome in a father and son with haploinsufficiency for FKBP6.