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Gene Protein Transcript Promoter Expression GO/PPI PubMed Cross reference

Gene information for FBN3 (Homo sapiens)
(Information is obtained from NCBI Gene database)
Entrez gene ID84467
Official gene symbolFBN3
Full namefibrillin 3
Aliases,KIAA1776,
Gene summaryThis gene encodes a protein that belongs to the fibrillin gene family. Fibrillins are extracellular matrix molecules that assemble into microfibrils in many connective tissues. This gene is most highly expressed in fetal tissues and its protein product is localized to extracellular microfibrils of developing skeletal elements, skin, lung, kidney, and skeletal muscle. This gene is potentially involved in Weill-Marchesani syndrome. While several transcript variants may exist for this gene, their full-length natures have not been described to date. [provided by RefSeq]
LocationChromosome: 19   Locus: 19p13
Gene position8212385 - 8130287  Map Viewer
Gene orientationminus
Gene size82099 bp
Gene sequence
OMIM ID608529