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Fibronectin type III domain-containing protein 10 (FNDC10)

Target: FNDC10
Molecular classification: Other (contains fibronectin type III domains; no established classification as receptor, enzyme, transporter, or ion channel)[1][2][5]

Overview

Fibronectin type III domain-containing protein 10 (FNDC10) is a membrane-associated protein encoded by a protein-coding gene located on human chromosome 1. FNDC10 contains fibronectin type III domains, which are often involved in protein–protein interactions including cell adhesion and signaling in other family members. However, for FNDC10 itself, neither a well-defined molecular function nor a role in specific biological pathways or as a drug target has been established in the current literature. The gene is mainly noted in genetic studies and has limited disease association with rare inherited diseases, but there is no evidence of it serving as a therapeutic target or biomarker in current biomedical research[1][3][5].

Other names: C1orf233fibronectin type-III domain-containing transmembrane protein C1orf233FNDC10

Biological functions

Unknown (no molecular function or specific biological process has been characterized for FNDC10 in human studies)[3][5]

Disease associations

Other (associated with rare genetic diseases such as Facial Hemiatrophy and 3-Methylglutaconic Aciduria, Type I; no established role in common disease categories)[1]

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