FKBP14, FKBP prolyl isomerase 14

FKBP14, FKBP prolyl isomerase 14

• 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]

• Gene Synonyms (peptidyl-prolyl cis-trans isomerase FKBP14, 22 kDa FK506-binding protein, 22 kDa FKBP, FK506 binding protein 14, 22 kDa, FK506-binding protein 14, FKBP-22, PPIase FKBP14, rotamase, EDSKMH, EDSKSCL2, FKBP22, IPBP12,)
• NCBI Gene ID: 55033
• Species: Homo sapiens (Human)
• UNIPROT ID#>>Q9NWM8
  UNIPROT ID#>>A0A090N7V8
• View the NCBI Database for this Gene »

Gene products are often involved in multiple pathways and networks within a living cell. Learn more about other interacting partners.

FKBP prolyl isomerase 14 interacts with:

• glucoside xylosyltransferase 1
  lysozyme like 2
  protein O-linked mannose N-acetylglucosaminyltransferase 2 (beta 1,4-)
  sperm acrosome associated 3
  transmembrane protein 237

Paste a protein or nucleic acid sequence in the box below to confirm that it matches this gene’s reference sequence(s). Click on a link under RELATED ORF CLONES to see how a sequence matches to an experimentally-validated ORF clone.