Target intelligence / Profile preview

Family with sequence similarity 187 member A (FAM187A)

Target
FAM187A
Molecular classification
Protein coding gene, Predicted Ig-like V-type domain-containing protein, Structured protein (possible membrane association), Other (function and family not definitively established)
01

Overview

**Family with sequence similarity 187 member A (FAM187A)** is a protein-coding gene in humans, located on chromosome 17 and encoding a 413-amino-acid polypeptide that is predicted to contain an immunoglobulin-like V-type domain[1][3][5]. The protein may be associated with membranes, but there is no verified experimental evidence for a defined structure or biological role[3][9]. Computational structure modeling by AlphaFold suggests the presence of ordered domains, but the proposed structural features have not been experimentally validated[3]. Function prediction is limited to computational analysis, which implies possible involvement in protein homodimerization; no specific cellular or physiological role has been established[1]. There are no reports directly connecting FAM187A to human diseases, pathophysiological pathways, or therapeutic intervention[1][4][5]. FAM187A has one important paralog, **FAM187B**, with similarly undefined function[1][5]. No drugs, biomarkers, or safety concerns have been identified. Scientific literature currently lacks experimental evidence for clear biological activity, molecular interactions, or clinical relevance, and the protein is not considered a validated therapeutic target. Alias and database accession numbers include RGD1307851, A6NFU0 (UniProt), ENSG00000214447 (Ensembl), and HGNC:35153[1][5][6].

Other names
FAM187AIg-like V-type domain-containing protein FAM187ARGD1307851A6NFU0 (UniProt identifier)
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Biological functions

Protein homodimerization activity (predicted by Gene Ontology annotation)Other (no experimentally confirmed molecular or cellular function)
03

Disease associations

Other (no established links to disease, cancer, inflammation, or any specific condition)

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