Target intelligence / Profile preview

Family with sequence similarity 219 member A (FAM219A)

Target
FAM219A
Molecular classification
Other (domain of unknown function, DUF), Protein-coding gene
01

Overview

Family with sequence similarity 219 member A (FAM219A) is a human protein encoded by the C9orf25 gene, located on chromosome 9 at 9p13.3. The protein is composed of 185 amino acids, with a molecular weight of 20.4 kDa and predicted cytosolic localization, lacking a signal sequence. It belongs to the FAM219 superfamily (Pfam PF15260), but remains a domain of unknown function, with no clear catalytic, receptor, or transport roles as of current knowledge. FAM219A is expressed in many tissues, with higher expression in the nervous, digestive, and male reproductive systems. Multiple transcript variants exist, with some encoding protein isoforms. FAM219A interacts with diverse proteins, some of which have disease associations, but it is not itself directly implicated in pathology. Experimental evidence for its biological process or molecular function is still lacking; therefore, it is currently categorized as a protein with unknown function and has no established therapeutic significance.

Other names
FAM219AC9orf25bA573M23.5FLJ39031protein FAM219Auncharacterized protein C9orf25family with sequence similarity 219 member A
02

Mechanism of action

None known. No mechanisms of drug action are described for this molecule.

03

Biological functions

Other (unknown, as currently there is no experimentally supported biological function annotation; the protein contains predicted phosphorylation sites and is cytosolic)
04

Disease associations

Other (has been linked to higher expression in metastatic cells and has disease-associated interactors, but there is no direct evidence for causality in disease)Associated with Kartagener Syndrome and Joubert Syndrome 22 through genetic studies, not as a direct disease driver

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