Homo sapiens CXXC repeat containing interactor of PDZ3 domain (CRIPT), - Nucleotide

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Biallelic variants in CRIPT cause a Rothmund-Thomson-like syndrome with increased cellular senescence. [Genet Med. 2023]
Biallelic variants in CRIPT cause a Rothmund-Thomson-like syndrome with increased cellular senescence.
Averdunk L, Huetzen MA, Moreno-Andrés D, Kalb R, McKee S, Hsieh TC, Seibt A, Schouwink M, Lalani S, Faqeih EA, et al. Genet Med. 2023 Jul; 25(7):100836. Epub 2023 Mar 31.
A novel biallelic CRIPT variant in a patient with short stature, microcephaly, and distinctive facial features. [Am J Med Genet A. 2023]
A novel biallelic CRIPT variant in a patient with short stature, microcephaly, and distinctive facial features.
Akalın A, Şimşek-Kiper PÖ, Taşkıran EZ, Karaosmanoğlu B, Utine GE, Boduroğlu K. Am J Med Genet A. 2023 Apr; 191(4):1119-1127. Epub 2023 Jan 11.
The Nse5/6-like SIMC1-SLF2 complex localizes SMC5/6 to viral replication centers. [Elife. 2022]
The Nse5/6-like SIMC1-SLF2 complex localizes SMC5/6 to viral replication centers.
Oravcová M, Nie M, Zilio N, Maeda S, Jami-Alahmadi Y, Lazzerini-Denchi E, Wohlschlegel JA, Ulrich HD, Otomo T, Boddy MN. Elife. 2022 Nov 14; 11. Epub 2022 Nov 14.

RefSeq protein product
See the reference protein sequence for cysteine-rich PDZ-binding protein (NP_054890.1).

Protein
Protein sequence from Nucleotide coding region
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Nucleotide