Homo sapiens tRNA isopentenylpyrophosphate transferase isoform 6 (TRIT - Nucleotide

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TRIT1 deficiency: Two novel patients with four novel variants. [Eur J Med Genet. 2022]
TRIT1 deficiency: Two novel patients with four novel variants.
Smol T, Brunelle P, Caumes R, Boute-Benejean O, Thuillier C, Figeac M, Ait-Yahya E, Bonte F, Mau-Them FT, Thauvin-Robinet C, et al. Eur J Med Genet. 2022 Nov; 65(11):104603. Epub 2022 Aug 29.
TRIT1 defect leads to a recognizable phenotype of myoclonic epilepsy, speech delay, strabismus, progressive spasticity, and normal lactate levels. [J Inherit Metab Dis. 2022]
TRIT1 defect leads to a recognizable phenotype of myoclonic epilepsy, speech delay, strabismus, progressive spasticity, and normal lactate levels.
Muylle E, Jiang H, Johnsen C, Byeon SK, Ranatunga W, Garapati K, Zenka RM, Preston G, Pandey A, Kozicz T, et al. J Inherit Metab Dis. 2022 Nov; 45(6):1039-1047. Epub 2022 Sep 21.
Scalable multiplex co-fractionation/mass spectrometry platform for accelerated protein interactome discovery. [Nat Commun. 2022]
Scalable multiplex co-fractionation/mass spectrometry platform for accelerated protein interactome discovery.
Havugimana PC, Goel RK, Phanse S, Youssef A, Padhorny D, Kotelnikov S, Kozakov D, Emili A. Nat Commun. 2022 Jul 13; 13(1):4043. Epub 2022 Jul 13.

RefSeq alternative splicing
See 5 reference mRNA sequence splice variants for the TRIT1 gene.

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Nucleotide