FMOD fibromodulin [ Homo sapiens (human) ]
Source: NCBI Gene (ID 2331)
Symbol: FMOD
Full name: fibromodulin
Gene type: protein coding
RefSeq status: REVIEWED
Organism: Homo sapiens
Also known as: FM; SLRR2E
Summary: Fibromodulin belongs to the family of small interstitial proteoglycans. The encoded protein possesses a central region containing leucine-rich repeats with 4 keratan sulfate chains, flanked by terminal domains containing disulphide bonds. Owing to the interaction with type I and type II collagen fibrils and in vitro inhibition of fibrillogenesis, the encoded protein may play a role in the assembly of extracellular matrix. It may also regulate TGF-beta activities by sequestering TGF-beta into the extracellular matrix. Sequence variations in this gene may be associated with the pathogenesis of high myopia. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jun 2013]
Expression: Broad expression in gall bladder (RPKM 78.8), fat (RPKM 77.4) and 22 other tissues
Orthologs: mouse
Gene size: 10495bp
Exon count: 4