Homo sapiens mRNA for 6.2 kd protein

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A hypomorphic variant in the translocase of the outer mitochondrial membrane complex subunit TOMM7 causes short stature and developmental delay. [HGG Adv. 2023]
A hypomorphic variant in the translocase of the outer mitochondrial membrane complex subunit TOMM7 causes short stature and developmental delay.
Young C, Batkovskyte D, Kitamura M, Shvedova M, Mihara Y, Akiba J, Zhou W, Hammarsjö A, Nishimura G, Yatsuga S, et al. HGG Adv. 2023 Jan 12; 4(1):100148. Epub 2022 Oct 4.
Autosomal recessive progeroid syndrome due to homozygosity for a TOMM7 variant. [J Clin Invest. 2022]
Autosomal recessive progeroid syndrome due to homozygosity for a TOMM7 variant.
Garg A, Keng WT, Chen Z, Sathe AA, Xing C, Kailasam PD, Shao Y, Lesner NP, Llamas CB, Agarwal AK, et al. J Clin Invest. 2022 Dec 1; 132(23). Epub 2022 Dec 1.
Protein interaction landscapes revealed by advanced in vivo cross-linking-mass spectrometry. [Proc Natl Acad Sci U S A. 2021]
Protein interaction landscapes revealed by advanced in vivo cross-linking-mass spectrometry.
Wheat A, Yu C, Wang X, Burke AM, Chemmama IE, Kaake RM, Baker P, Rychnovsky SD, Yang J, Huang L. Proc Natl Acad Sci U S A. 2021 Aug 10; 118(32).

Homo sapiens mRNA for 6.2 kd protein
Homo sapiens mRNA for 6.2 kd protein
gi|4468340|emb|AJ011007.1|

Nucleotide
Homo sapiens mRNA; cDNA DKFZp727G051 (from clone DKFZp727G051); partial cds
Homo sapiens mRNA; cDNA DKFZp727G051 (from clone DKFZp727G051); partial cds
gi|5911950|emb|AL117477.1|

Nucleotide

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Nucleotide