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Family with sequence similarity 174 member A (FAM174A)

Target
FAM174A
Molecular classification
Other (unclassified membrane protein; contains a domain of unknown function, DUF1180)
01

Overview

Family with sequence similarity 174 member A (FAM174A) is a poorly characterized membrane protein carrying a domain of unknown function (DUF1180). It is expressed in various tissues and has been implicated in diverse biological processes, including cholesterol and lipid metabolism, metabolic homeostasis, and developmental pigmentation in animal models. Recent studies have connected it to oncogenic roles, notably through the formation of fusion genes such as FAM174A-WWC1 in early-onset colorectal cancer, where the fusion protein disrupts cell adhesion and perturbs Hippo pathway signaling, increasing tumorigenic potential. Genome-wide analyses also suggest its involvement in metabolic syndrome and rare variants in neurodegenerative disease, but direct therapeutic targeting, established disease biomarkers, or drug interactions for FAM174A remain undocumented. Its precise mechanism(s) and molecular partners remain largely unknown and warrant further research.

Other names
Membrane protein FAM174ANS5ATP6TMEM157UNQ1912/PRO4371HCV NS5A-transactivated protein 6UNQ1912hepatitis C virus NS5A-transactivated protein 6hepatitis C virus nonstructural protein 5A trans-activated protein 6Transmembrane protein 157HGS_RE408
02

Biological functions

Cholesterol and lipid regulation (modulates low-density lipoprotein receptor levels and intracellular cholesterol balance)Metabolic homeostasisDevelopmental pigmentation (associated with pigmentation traits in animals, e.g., earlobe color in chickens)Potential oncogenic transformation (especially when fused with other genes, such as WWC1)Possible implication in neurodegenerative diseaseCellular adhesion and cytoskeletal dynamics (as part of a fusion protein)
03

Disease associations

Cancer (notably early-onset colorectal cancer via FAM174A-WWC1 fusion)Metabolic syndrome (implicated in obesity and cholesterol deregulation in animal models)Neurodegenerative disease (novel candidate in Parkinson's disease genetic studies)Other (pigmentation disorders in animals)

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