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FKBP14

Official Full Name
FKBP prolyl isomerase 14
Organism
Homo sapiens
GeneID
55033
Background
The protein encoded by this gene is a member of the FK506-binding protein family of peptidyl-prolyl cis-trans isomerases. The encoded protein is found in the lumen of the endoplasmic reticulum, where it is thought to accelerate protein folding. Defects in this gene are a cause of a type of Ehlers-Danlos syndrome (EDS). Both a protein-coding variant and noncoding variants are transcribed from this gene. [provided by RefSeq, Mar 2012]
Synonyms
EDSKMH; FKBP22; IPBP12; EDSKSCL2;

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