peptidyl-prolyl cis-trans isomerase FKBP10 isoform X2 [Homo sapiens]

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Presentation of Rare Phenotypes Associated with the FKBP10 Gene. [Genes (Basel). 2024]
Presentation of Rare Phenotypes Associated with the FKBP10 Gene.
Merkuryeva ES, Markova TV, Kenis VM, Agranovich OE, Dan IM, Kotalevskaya YY, Shchagina OA, Ryzhkova OP, Fomenko SS, Dadali EL, et al. Genes (Basel). 2024 May 23; 15(6). Epub 2024 May 23.
Mutation In Fkbp10 Gene Cause Bruck Syndrome 1 (Brks1) In A Pakistani Family Of Pashtun Origin. [J Ayub Med Coll Abbottabad. 2023]
Mutation In Fkbp10 Gene Cause Bruck Syndrome 1 (Brks1) In A Pakistani Family Of Pashtun Origin.
Tauseef U, Ibrahim M, Noor N, Hanif M. J Ayub Med Coll Abbottabad. 2023 Apr-Jun; 35(2):341-347.
Clinical features and molecular characterization of Chinese patients with FKBP10 variants. [Mol Genet Genomic Med. 2023]
Clinical features and molecular characterization of Chinese patients with FKBP10 variants.
Tan Z, Shek HT, Chen P, Dong Z, Zhou Y, Yin S, Qiu A, Dong L, Gao B, To MKT. Mol Genet Genomic Med. 2023 Apr; 11(4):e2122. Epub 2023 Jan 19.

RefSeq genomic sequence
See the genomic reference sequence for the FKBP10 gene (NG_015860.1).
RefSeq mRNA
See reference mRNA sequence for the FKBP10 gene (XM_011525100.3).
RefSeq protein isoforms
See 7 reference sequence protein isoforms for the FKBP10 gene.

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Protein