FKBP14 抗体
(FK506 Binding Protein 14, 22 KDa (FKBP14))
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].
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Latest Publications for our FKBP14 抗体
: "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).
: "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).
Aliases for FKBP14 抗体
FK506 binding protein 14 (FKBP14) 抗体FK506 binding protein 14 L homeolog (fkbp14.L) 抗体
FK506 binding protein 14 (fkbp14) 抗体
FK506 binding protein 14, 22 kDa (FKBP14) 抗体
peptidyl-prolyl cis-trans isomerase FKBP14 (LOC100228355) 抗体
FK506 binding protein 14 (Fkbp14) 抗体
BC029109 抗体
EDSKMH 抗体
FKBP-14 抗体
FKBP22 抗体
IPBP12 抗体
MGC81908 抗体
MGC89927 抗体
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