Mus musculus talin 2 mRNA, partial cds

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Neuron-specific protein network mapping of autism risk genes identifies shared biological mechanisms and disease-relevant pathologies. [Cell Rep. 2022]
Neuron-specific protein network mapping of autism risk genes identifies shared biological mechanisms and disease-relevant pathologies.
Murtaza N, Cheng AA, Brown CO, Meka DP, Hong S, Uy JA, El-Hajjar J, Pipko N, Unda BK, Schwanke B, et al. Cell Rep. 2022 Nov 22; 41(8):111678.
Loss of talin in cardiac fibroblasts results in augmented ventricular cardiomyocyte hypertrophy in response to pressure overload. [Am J Physiol Heart Circ Physio...]
Loss of talin in cardiac fibroblasts results in augmented ventricular cardiomyocyte hypertrophy in response to pressure overload.
Noll NA, Riley LA, Moore CS, Zhong L, Bersi MR, West JD, Zent R, Merryman WD. Am J Physiol Heart Circ Physiol. 2022 May 1; 322(5):H857-H866. Epub 2022 Mar 25.
Genetic resiliency associated with dominant lethal TPM1 mutation causing atrial septal defect with high heritability. [Cell Rep Med. 2022]
Genetic resiliency associated with dominant lethal TPM1 mutation causing atrial septal defect with high heritability.
Teekakirikul P, Zhu W, Xu X, Young CB, Tan T, Smith AM, Wang C, Peterson KA, Gabriel GC, Ho S, et al. Cell Rep Med. 2022 Feb 15; 3(2):100501. Epub 2022 Feb 15.

RefSeq alternative splicing
See 15 reference mRNA sequence splice variants for the Tln2 gene.

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Nucleotide