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 Association of IL-17 and PlGF/sENG Ratio in Pre-Eclampsia and Adverse Pregnancy Outcomes. [Int J Environ Res Public Healt...]
The Association of IL-17 and PlGF/sENG Ratio in Pre-Eclampsia and Adverse Pregnancy Outcomes.
Darmochwal-Kolarz D, Chara A. Int J Environ Res Public Health. 2022 Dec 31; 20(1). Epub 2022 Dec 31.

Protein
Protein sequence from Nucleotide coding region
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RNA
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Nucleotide