Entity Details

Primary name FIBP
Entity type gene
Source Source Link

Details

PrimaryID9158
RefseqGeneNG_047103
SymbolFIBP
NameFGF1 intracellular binding protein
Chromosome11
Location11q13.1
TaxID9606
Statuslive
SourceGenomegenomic
SourceOriginnatural
CreationDate1999-06-07
ModificationDate2021-06-11

Ontological Relatives

UniProt IDsFIBP_HUMAN

GO terms

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GOName
GO:0005634 nucleus
GO:0005739 mitochondrion
GO:0008543 fibroblast growth factor receptor signaling pathway
GO:0012505 endomembrane system
GO:0016020 membrane
GO:0016607 nuclear speck
GO:0017134 fibroblast growth factor binding
GO:0070527 platelet aggregation

Diseases

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Disease IDSourceNameDescription
617107 OMIMThauvin-Robinet-Faivre syndrome (TROFAS)A rare autosomal recessive syndrome characterized by generalized overgrowth, developmental delay, learning disabilities, and variable congenital abnormalities including congenital heart defects, renal dysplasia, and skeletal defects. The disease is caused by variants affecting the gene represented in this entry.