Homo sapiens tenascin R (restrictin, janusin), mRNA (cDNA clone MGC:14 - Nucleotide

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Loss of TNR causes a nonprogressive neurodevelopmental disorder with spasticity and transient opisthotonus. [Genet Med. 2020]
Loss of TNR causes a nonprogressive neurodevelopmental disorder with spasticity and transient opisthotonus.
Wagner M, Lévy J, Jung-Klawitter S, Bakhtiari S, Monteiro F, Maroofian R, Bierhals T, Hempel M, Elmaleh-Bergès M, Kitajima JP, et al. Genet Med. 2020 Jun; 22(6):1061-1068. Epub 2020 Feb 26.
DCAF8, a novel MuRF1 interaction partner, promotes muscle atrophy. [J Cell Sci. 2019]
DCAF8, a novel MuRF1 interaction partner, promotes muscle atrophy.
Nowak M, Suenkel B, Porras P, Migotti R, Schmidt F, Kny M, Zhu X, Wanker EE, Dittmar G, Fielitz J, et al. J Cell Sci. 2019 Sep 6; 132(17). Epub 2019 Sep 6.
A case-control genome-wide association study of ADHD discovers a novel association with the tenascin R (TNR) gene. [Transl Psychiatry. 2018]
A case-control genome-wide association study of ADHD discovers a novel association with the tenascin R (TNR) gene.
Hawi Z, Yates H, Pinar A, Arnatkeviciute A, Johnson B, Tong J, Pugsley K, Dark C, Pauper M, Klein M, et al. Transl Psychiatry. 2018 Dec 18; 8(1):284. Epub 2018 Dec 18.

RefSeq alternative splicing
See 2 reference mRNA sequence splice variants for the TNR gene.

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Nucleotide