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Results for "MFN2": 1 gene, 4 gene sets

Name

MFN2 Gene

mitofusin 2

This gene encodes a mitochondrial membrane protein that participates in mitochondrial fusion and contributes to the maintenance and operation of the mitochondrial network. This protein is involved in the regulation of vascular smooth muscle cell proliferation, and it may play a role in the pathophysiology of obesity. Mutations in this gene cause Charcot-Marie-Tooth disease type 2A2, and hereditary motor and sensory neuropathy VI, which are both disorders of the peripheral nervous system. Defects in this gene have also been associated with early-onset stroke. Two transcript variants encoding the same protein have been identified. [provided by RefSeq, Jul 2008]

mfn2 Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term mfn2 in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

MFN2 Gene Set

From Pathway Commons Protein-Protein Interactions

interacting proteins for MFN2 from the Pathway Commons Protein-Protein Interactions dataset.

MFN2 Gene Set

From CM4AI KOLF21J CRISPRi Gene Perturbation Atlas

genes differentially expressed following the MFN2 gene perturbation from the CM4AI KOLF21J CRISPRi Gene Perturbation Atlas.

Effects of MFN2 mutation Gene Set

From WikiPathways Pathways 2024

proteins participating in the Effects of MFN2 mutation pathway from the WikiPathways Pathways 2024 dataset.