tetratricopeptide repeat domain 5, isoform CRA_c [Homo sapiens]

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TTC5 syndrome: Clinical and molecular spectrum of a severe and recognizable condition. [Am J Med Genet A. 2022]
TTC5 syndrome: Clinical and molecular spectrum of a severe and recognizable condition.
Musante L, Faletra F, Meier K, Tomoum H, Najarzadeh Torbati P, Blair E, North S, Gärtner J, Diegmann S, Beiraghi Toosi M, et al. Am J Med Genet A. 2022 Sep; 188(9):2652-2665. Epub 2022 Jun 7.
Bi-allelic TTC5 variants cause delayed developmental milestones and intellectual disability. [J Med Genet. 2021]
Bi-allelic TTC5 variants cause delayed developmental milestones and intellectual disability.
Rasheed A, Gumus E, Zaki M, Johnson K, Manzoor H, LaForce G, Ross D, McEvoy-Venneri J, Stanley V, Lee S, et al. J Med Genet. 2021 Apr; 58(4):237-246. Epub 2020 May 21.
Evaluation of the Role of p53 Tumour Suppressor Posttranslational Modifications and TTC5 Cofactor in Lung Cancer. [Int J Mol Sci. 2021]
Evaluation of the Role of p53 Tumour Suppressor Posttranslational Modifications and TTC5 Cofactor in Lung Cancer.
Alhebshi H, Tian K, Patnaik L, Taylor R, Bezecny P, Hall C, Muller PAJ, Safari N, Creamer DPM, Demonacos C, et al. Int J Mol Sci. 2021 Dec 7; 22(24). Epub 2021 Dec 7.

RefSeq protein
See the reference protein sequence for tetratricopeptide repeat protein 5 (NP_612385.2).

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