Homo sapiens tRNA mitochondrial 2-thiouridylase (TRMU), transcript var - Nucleotide

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Pathological mutations promote proteolysis of mitochondrial tRNA-specific 2-thiouridylase 1 (MTU1) via mitochondrial caseinolytic peptidase (CLPP). [Nucleic Acids Res. 2024]
Pathological mutations promote proteolysis of mitochondrial tRNA-specific 2-thiouridylase 1 (MTU1) via mitochondrial caseinolytic peptidase (CLPP).
Ahmad RNR, Zhang LT, Morita R, Tani H, Wu Y, Chujo T, Ogawa A, Harada R, Shigeta Y, Tomizawa K, et al. Nucleic Acids Res. 2024 Feb 9; 52(3):1341-1358.
Antagonistic roles of canonical and Alternative-RPA in disease-associated tandem CAG repeat instability. [Cell. 2023]
Antagonistic roles of canonical and Alternative-RPA in disease-associated tandem CAG repeat instability.
Gall-Duncan T, Luo J, Jurkovic CM, Fischer LA, Fujita K, Deshmukh AL, Harding RJ, Tran S, Mehkary M, Li V, et al. Cell. 2023 Oct 26; 186(22):4898-4919.e25. Epub 2023 Oct 11.
TRMU Deficiency. [GeneReviews(®). 1993]
TRMU Deficiency.
Reinhart M, Muraresku C, Ganetzky R. GeneReviews(®). 1993-2024. 2023 May 11

RefSeq alternative splicing
See 15 reference mRNA sequence splice variants for the TRMU gene.
RefSeq protein product
See the reference protein sequence for mitochondrial tRNA-specific 2-thiouridylase 1 isoform f (NP_001269713.1).

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Protein sequence from Nucleotide coding region
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BioProjects for Gene (Select 80000) (4)
BioProject
SPTB spectrin beta, erythrocytic [Homo sapiens]
SPTB spectrin beta, erythrocytic [Homo sapiens]
Gene ID:6710

Gene
Gene Links for GEO Profiles (Select 56908996) (1)
Gene
Homo sapiens isolate CHM13 chromosome 9, alternate assembly T2T-CHM13v2.0
Homo sapiens isolate CHM13 chromosome 9, alternate assembly T2T-CHM13v2.0
gi|2194973615|gnl|ASM:GCF_009914825 f|NC_060933.1||gpp|GPC_000012748.1||gnl|NCBI_GENOMES|119569

Nucleotide
GRAMD1A GRAM domain containing 1A [Homo sapiens]
GRAMD1A GRAM domain containing 1A [Homo sapiens]
Gene ID:57655

Gene

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Nucleotide