Target intelligence / Profile preview

Family with sequence similarity 81 member A (FAM81A)

Target
FAM81A
Molecular classification
Other (postsynaptic scaffold protein), Intracellular structural/scaffold protein, Not a receptor, enzyme, transporter, or transcription factor
01

Overview

Family with sequence similarity 81 member A (FAM81A) is a protein selectively expressed in the adult brain, specifically at the postsynaptic density of excitatory neurons, particularly in the cerebral cortex and hippocampus[3][5][6][7]. It facilitates the condensation and assembly of postsynaptic proteins, likely regulating them through liquid-liquid phase separation, and is implicated in synaptic organization and potentially in synaptic plasticity[1][2][3][5][6][7]. FAM81A is not known to function as a conventional receptor, enzyme, or transporter, and currently, there are no known drugs that specifically target it. Alterations in the genomic region of FAM81A have been observed in certain cancers, e.g., non-muscle invasive bladder cancer, and it has been studied as a candidate gene in pathological mineralization and neuronal circuit research, but a direct disease-causing or therapeutic target role remains unproven[5]. FAM81A is a postsynaptic density-associated scaffold protein, highly brain-selective, involved in organizing key synaptic assemblies and supporting adult synaptic function. It is not currently considered a classical therapeutic target, and there is no evidence for direct clinical modulation or drug targeting[1][3][5][6][7].

Other names
Protein FAM81AMGC26690FA81A_HUMANQ8TBF8GC15P057518GC15P059730GC15P036552GC15P059664
02

Biological functions

Synaptic organizationModulation of postsynaptic densityFacilitation of liquid-liquid phase separation in postsynaptic densityPotential roles in neuronal activity and dendritic spine morphogenesis
03

Disease associations

Potential biomarker or candidate gene in non-muscle invasive bladder cancer (by copy number variation)Association with synovial calcification in joint injury modelsPossible involvement in neural function and neurological disease (no direct evidence for specific diseases as a driver gene)
04

Biomarkers

Possible biomarker in non-muscle-invasive bladder cancer (by genomic copy number variation)Used as a reporter in mouse models for visual processing studies

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