FGFRL1 fibroblast growth factor receptor like 1 [ Homo sapiens (human) ]
Source: NCBI Gene (ID 53834)
Source: NCBI Gene (ID 53834)
Symbol: FGFRL1
Full name: fibroblast growth factor receptor like 1
Gene type: protein coding
RefSeq status: REVIEWED
Organism: Homo sapiens
Also known as: FGFR-5; FGFR5; FHFR
Summary: The protein encoded by this gene is a member of the fibroblast growth factor receptor (FGFR) family, where amino acid sequence is highly conserved between members and throughout evolution. FGFR family members differ from one another in their ligand affinities and tissue distribution. A full-length representative protein would consist of an extracellular region, composed of three immunoglobulin-like domains, a single hydrophobic membrane-spanning segment and a cytoplasmic tyrosine kinase domain. The extracellular portion of the protein interacts with fibroblast growth factors, setting in motion a cascade of downstream signals, ultimately influencing mitogenesis and differentiation. A marked difference between this gene product and the other family members is its lack of a cytoplasmic tyrosine kinase domain. The result is a transmembrane receptor that could interact with other family members and potentially inhibit signaling. Multiple alternatively spliced transcript variants encoding the same isoform have been found for this gene. [provided by RefSeq, Jul 2008]
Expression: Ubiquitous expression in thyroid (RPKM 21.2), fat (RPKM 15.4) and 25 other tissues
Orthologs: mouse
Gene size: 16687bp
Exon count: 10