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- Table of Contents
Facts about Peptidyl-prolyl cis-trans isomerase FKBP14.
May also target type VI and type X collagens. .
Human | |
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Gene Name: | FKBP14 |
Uniprot: | Q9NWM8 |
Entrez: | 55033 |
Belongs to: |
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No superfamily |
22 kDa FK506-binding protein; EC 5.2.1.8; FK506 binding protein 14 (22 kDa); FK506 binding protein 14, 22 kDa; FK506-binding protein 14; FKBP-14; FKBP-22; FKBP22PPIase FKBP14; FLJ20731; peptidyl-prolyl cis-trans isomerase FKBP14,22 kDa FKBP; rotamase
Mass (kDA):
24.172 kDA
Human | |
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Location: | 7p14.3 |
Sequence: | 7; NC_000007.14 (30010587..30026702, complement) |
Endoplasmic reticulum lumen.
PMID: 22265013 by Baumann M., et al. Mutations in FKBP14 cause a variant of Ehlers-Danlos syndrome with progressive kyphoscoliosis, myopathy, and hearing loss.
PMID: 24821723 by Ishikawa Y., et al. A substrate preference for the rough endoplasmic reticulum resident protein FKBP22 during collagen biosynthesis.