TSA: Macaca mulatta Mamu_379239 mRNA sequence

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Heterozygous MAP3K20 variants cause ectodermal dysplasia, craniosynostosis, sensorineural hearing loss, and limb anomalies. [Hum Genet. 2024]
Heterozygous MAP3K20 variants cause ectodermal dysplasia, craniosynostosis, sensorineural hearing loss, and limb anomalies.
Brooks D, Burke E, Lee S, Eble TN, O'Leary M, Osei-Owusu I, Rehm HL, Dhar SU, Emrick L, Bick D, et al. Hum Genet. 2024 Mar; 143(3):279-291. Epub 2024 Mar 7.
Myofibrillar myopathy hallmarks associated with ZAK deficiency. [Hum Mol Genet. 2023]
Myofibrillar myopathy hallmarks associated with ZAK deficiency.
Stonadge A, Genzor AV, Russell A, Hamed MF, Romero N, Evans G, Pownall ME, Bekker-Jensen S, Blanco G. Hum Mol Genet. 2023 Aug 26; 32(17):2751-2770.
A central chaperone-like role for 14-3-3 proteins in human cells. [Mol Cell. 2023]
A central chaperone-like role for 14-3-3 proteins in human cells.
Segal D, Maier S, Mastromarco GJ, Qian WW, Nabeel-Shah S, Lee H, Moore G, Lacoste J, Larsen B, Lin ZY, et al. Mol Cell. 2023 Mar 16; 83(6):974-993.e15.

RefSeq alternative splicing
See 3 reference mRNA sequence splice variants for the MAP3K20 gene.

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Nucleotide