Homo sapiens SLIT and NTRK like family member 2 (SLITRK2), transcript - Nucleotide

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SLITRK2 variants associated with neurodevelopmental disorders impair excitatory synaptic function and cognition in mice. [Nat Commun. 2022]
SLITRK2 variants associated with neurodevelopmental disorders impair excitatory synaptic function and cognition in mice.
El Chehadeh S, Han KA, Kim D, Jang G, Bakhtiari S, Lim D, Kim HY, Kim J, Kim H, Wynn J, et al. Nat Commun. 2022 Jul 15; 13(1):4112. Epub 2022 Jul 15.
Slitrk2 deficiency causes hyperactivity with altered vestibular function and serotonergic dysregulation. [iScience. 2022]
Slitrk2 deficiency causes hyperactivity with altered vestibular function and serotonergic dysregulation.
Katayama KI, Morimura N, Kobayashi K, Corbett D, Okamoto T, Ornthanalai VG, Matsunaga H, Fujita W, Matsumoto Y, Akagi T, et al. iScience. 2022 Jul 15; 25(7):104604. Epub 2022 Jun 14.
The Functional Proximal Proteome of Oncogenic Ras Includes mTORC2. [Mol Cell. 2019]
The Functional Proximal Proteome of Oncogenic Ras Includes mTORC2.
Kovalski JR, Bhaduri A, Zehnder AM, Neela PH, Che Y, Wozniak GG, Khavari PA. Mol Cell. 2019 Feb 21; 73(4):830-844.e12. Epub 2019 Jan 10.

RefSeq alternative splicing
See 20 reference mRNA sequence splice variants for the SLITRK2 gene.
RefSeq protein product
See the reference protein sequence for SLIT and NTRK-like protein 2 precursor (NP_001137478.1).

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Protein sequence from Nucleotide coding region
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Nucleotide