Homo sapiens RUNX family transcription factor 2 (RUNX2), transcript va - Nucleotide

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Hypomethylation of the RUNX2 Gene Is a New Potential Biomarker of Primary Osteoporosis in Men and Women. [Int J Mol Sci. 2024]
Hypomethylation of the RUNX2 Gene Is a New Potential Biomarker of Primary Osteoporosis in Men and Women.
Yalaev B, Tyurin A, Akhiiarova K, Khusainova R. Int J Mol Sci. 2024 Jul 3; 25(13). Epub 2024 Jul 3.
FOXO1 regulates RUNX2 ubiquitination through SMURF2 in calcific aortic valve disease. [Redox Biol. 2024]
FOXO1 regulates RUNX2 ubiquitination through SMURF2 in calcific aortic valve disease.
Jiang C, Yao D, Liu Z, Zheng Y, Chen M, Yim WY, Zheng Q, Zhang T, Fan L, Fan Z, et al. Redox Biol. 2024 Jul; 73:103215. Epub 2024 May 27.
METTL3 Promotes Osteogenic Differentiation of Human Periodontal Ligament Stem Cells through IGF2BP1-Mediated Regulation of Runx2 Stability. [Int J Med Sci. 2024]
METTL3 Promotes Osteogenic Differentiation of Human Periodontal Ligament Stem Cells through IGF2BP1-Mediated Regulation of Runx2 Stability.
Sun X, Meng X, Piao Y, Dong S, Dong Q. Int J Med Sci. 2024; 21(4):664-673. Epub 2024 Feb 4.

RefSeq alternative splicing
See 4 reference mRNA sequence splice variants for the RUNX2 gene.
RefSeq protein product
See the reference protein sequence for runt-related transcription factor 2 isoform b (NP_001015051.3).

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Protein sequence from Nucleotide coding region
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Nucleotide