Homo sapiens hFKBP65 mRNA for FK506 binding protein, complete cds, cDN - Nucleotide

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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 alternative splicing
See 7 reference mRNA sequence splice variants for the FKBP10 gene.

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Homo sapiens hFKBP65 mRNA for FK506 binding protein, complete cds, cDNA:PSEC0056...
Homo sapiens hFKBP65 mRNA for FK506 binding protein, complete cds, cDNA:PSEC0056 from clone:NT2RP2000565
gi|12231181|dbj|AB045981.1|

Nucleotide
Homologene neighbors for GEO Profiles (Select 130177552) (0)
GEO Profiles
Component Of for Nucleotide (Select 2494428408) (0)
Nucleotide
Taxonomy Links for Nucleotide (Select 2494428408) (1)
Taxonomy
Concise Conserved Domain Links for Protein (Select 7657554) (1)
Conserved Domains

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Nucleotide