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Gene : FNBP1 Homo sapiens

Name  ? formin binding protein 1 Cytological Location  9q34.11
Brief Description  formin binding protein 1
Description  The protein encoded by this gene is a member of the formin-binding-protein family. The protein contains an N-terminal Fer/Cdc42-interacting protein 4 (CIP4) homology (FCH) domain followed by a coiled-coil domain, a proline-rich motif, a second coiled-coil domain, a Rho family protein-binding domain (RBD), and a C-terminal SH3 domain. This protein binds sorting nexin 2 (SNX2), tankyrase (TNKS), and dynamin; an interaction between this protein and formin has not been demonstrated yet in human. [provided by RefSeq, Jul 2008]
  • synonyms:
  • FBP17,
  • AB011126,
  • uc004byw.2,
  • FBP17,
  • KIAA0554,
  • HGNC:17069,
  • NM_001363755,
  • OTTHUMG00000020800,
  • FNBP1
  • identifiers:
  • 23048,
  • ENSG00000187239,
  • FNBP1

Genome feature

Region: gene ? Length: 166660  
Location: 9:129887187-130053846 reverse strand Cyto location: 9q34.11

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Gene -> HPO annotation (Human Phenotype Ontology)

Mouse Gene --> Allele [Phenotype]


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0 Diseases

Gene (Hum OR Rat) --> Mouse Allele (Phenotype)

Gene --> Alleles and Disease (clinVar data)

Gene -> HPO annotation (Human Phenotype Ontology)

Mouse Gene --> Allele [Phenotype]


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Gene(s) --> Significant SNPs (GTex data)

Gene Ontology

Gene --> GO terms.



3753 SN Ps

5 Cross References

17 Data Sets

7 Homologues

0 Located Features

97 Rna Seq Results