Target intelligence / Profile preview

Family with sequence similarity 156 member A (FAM156A)

Target
FAM156A
Molecular classification
Other (predicted nuclear protein, not a classical receptor, enzyme, transporter, or ion channel)[2][1]
01

Overview

Family with sequence similarity 156 member A (FAM156A), also known as Transmembrane protein 29 (TMEM29), is a predicted nuclear envelope-localized protein believed to enable methylated histone binding activity, though precise molecular function remains incompletely characterized[2][1]. FAM156A is expressed in various tissues, with prominent expression in testes, brain, and kidney in mouse models, and displays several splice variants including both coding and non-coding transcripts[1]. Experimental evidence suggests FAM156A responds to cellular stress (e.g., oxygen-glucose deprivation) and is associated with apoptosis, particularly in neuronal cells, potentially linking it to adaptive stress response and cell death pathways[1]. While not currently considered a therapeutic target, it is investigated as a candidate gene in neurodevelopmental disorders, such as X-linked mental retardation, and as a possible prognostic biomarker in lung adenocarcinoma patients[2]. There is currently no known drug targeting FAM156A, nor established mechanisms of action or specific safety concerns related to the modulation of this molecule[2][1].

Other names
TMEM29PRO0659Transmembrane protein 29PP12994
02

Biological functions

Predicted methylated histone binding activity[2]Implicated in neurodevelopment and cognitive function as a candidate gene in X-linked mental retardation (XLMR)[2]Possible involvement in cellular response to injury (hypoxic-ischemic insult); may play a role in adaptive cellular response and programmed cell death within the nucleus[1]
03

Disease associations

Candidate gene in X-linked mental retardation (neurodevelopmental disorders)[2]Marker in lung adenocarcinoma context for prognosis (altered expression in non-involved lung tissue)[2]Possible relevance in hypoxic-ischemic encephalopathy (based on expression changes after brain injury in animal models)[1]
04

Biomarkers

Proposed as a prognostic biomarker in lung adenocarcinoma based on expression signature in non-involved lung tissue[2]

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