mitochondrial import receptor subunit TOM7 homolog [Homo sapiens]

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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.
Cloning and characterization of the human novel gene encoding 6.2 kDa protein highly expressed upon ultraviolet irradiation in DNA-PK-deleted human glioma M059J cells. [DNA Seq. 1999]
Cloning and characterization of the human novel gene encoding 6.2 kDa protein highly expressed upon ultraviolet irradiation in DNA-PK-deleted human glioma M059J cells.
Lee JS. DNA Seq. 1999; 10(3):195-8.
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.

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Ensembl [Ensembl]
Ensembl
GlyGen glycoinformatics resource [GlyGen glycoinformatics resou...]
GlyGen glycoinformatics resource
OncoMX cancer biomarker resource [OncoMX cancer biomarker resou...]
OncoMX cancer biomarker resource
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reagents [ExactAntigen/Labome]
reagents
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