(FK506 Binding Protein 14, 22 KDa (FKBP14))
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Latest Publications for our FKBP14 products: "Mutations in FKBP14 cause a variant of Ehlers-Danlos syndrome with progressive kyphoscoliosis, myopathy, and hearing loss. ..." in: American journal of human genetics, Vol. 90, Issue 2, pp. 201-16, (2012) (PubMed).
: "Genomic organization of mouse and human 65 kDa FK506-binding protein genes and evolution of the FKBP multigene family." in: Genomics, Vol. 79, Issue 6, pp. 881-9, (2002) (PubMed).
Synonyms and alternative names related to FKBP14FK506 binding protein 14 (FKBP14), FK506 binding protein 14 L homeolog (fkbp14.L), FK506 binding protein 14 (fkbp14), FK506 binding protein 14, 22 kDa (FKBP14), peptidyl-prolyl cis-trans isomerase FKBP14 (LOC100228355), FK506 binding protein 14 (Fkbp14), BC029109, EDSKMH, FKBP-14, FKBP22, IPBP12, MGC81908, MGC89927
Protein level used designations for FKBP14
- FK506 binding protein 14, 22 kDa
- FK506-binding protein 14
- PPIase FKBP14
- peptidyl-prolyl cis-trans isomerase FKBP14
- 22 kDa FK506-binding protein
- 22 kDa FKBP
Did you look for something else?
- Fission 1
- Filamin A Interacting Protein 1
- Filamin A
- Filamentous Hemagglutinin