Bos taurus Gene: BT.24497
Summary
InnateDB Gene IDBG-635905.3
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol BT.24497
Gene Name FGFR1 oncogene partner
Synonyms
Species Bos taurus
Ensembl Gene ENSBTAG00000014495
Encoded Proteins
FGFR1 oncogene partner
Protein Structure
Useful resources Stemformatics EHFPI ImmGen
Entrez Gene
Summary This gene does not have any Entrez summary - the following is the summary from its human ortholog ENSG00000213066:
This gene encodes a largely hydrophilic protein postulated to be a leucine-rich protein family member. A t(6;8)(q27;p11) chromosomal translocation, fusing this gene and the fibroblast growth factor receptor 1 (FGFR1) gene, has been found in cases of myeloproliferative disorder. The resulting chimeric protein contains the N-terminal leucine-rich region of this encoded protein fused to the catalytic domain of FGFR1. This gene is thought to play an important role in normal proliferation and differentiation of the erythroid lineage. Alternatively spliced transcript variants that encode different proteins have been identified. [provided by RefSeq, Jul 2008]
This gene encodes a largely hydrophilic centrosomal protein that is required for anchoring microtubules to subcellular structures. A t(6;8)(q27;p11) chromosomal translocation, fusing this gene and the fibroblast growth factor receptor 1 (FGFR1) gene, has been found in cases of myeloproliferative disorder. The resulting chimeric protein contains the N-terminal leucine-rich region of this encoded protein fused to the catalytic domain of FGFR1. Alterations in this gene may also be associated with Crohn\'s disease, Graves\' disease, and vitiligo. Alternatively spliced transcript variants that encode different proteins have been identified. [provided by RefSeq, Jul 2013]
Gene Information
Type Protein coding
Genomic Location Chromosome 9:103355965-103381325
Strand Forward strand
Band
Transcripts
ENSBTAT00000019271 ENSBTAP00000019271
Interactions
Number of Interactions This gene and/or its encoded proteins are associated with 0 experimentally validated interaction(s) in this database.
They are also associated with 12 interaction(s) predicted by orthology.
Predicted by orthology
Total 12 [view]
Gene Ontology

Molecular Function
Accession GO Term
GO:0005515 protein binding
GO:0019901 protein kinase binding
GO:0030292 protein tyrosine kinase inhibitor activity
GO:0042803 protein homodimerization activity
Biological Process
GO:0006469 negative regulation of protein kinase activity
GO:0008284 positive regulation of cell proliferation
GO:0030307 positive regulation of cell growth
GO:0030335 positive regulation of cell migration
GO:0034453 microtubule anchoring
GO:0061099 negative regulation of protein tyrosine kinase activity
Cellular Component
GO:0005634 nucleus
GO:0005813 centrosome
GO:0005815 microtubule organizing center
GO:0048471 perinuclear region of cytoplasm
Orthologs
Species
Mus musculus
Homo sapiens
Gene ID
Gene Order
Pathway Predictions based on Human Orthology Data
NETPATH
REACTOME
Recruitment of mitotic centrosome proteins and complexes pathway
G2/M Transition pathway
Cell Cycle, Mitotic pathway
Disease pathway
Loss of Nlp from mitotic centrosomes pathway
Signaling by FGFR in disease pathway
Cell Cycle pathway
Mitotic G2-G2/M phases pathway
Loss of proteins required for interphase microtubule organization� from the centrosome pathway
Regulation of PLK1 Activity at G2/M Transition pathway
Signaling by FGFR mutants pathway
Signaling by FGFR1 mutants pathway
Signaling by FGFR1 fusion mutants pathway
Centrosome maturation pathway
Regulation of PLK1 Activity at G2/M Transition pathway
Loss of Nlp from mitotic centrosomes pathway
Loss of proteins required for interphase microtubule organization� from the centrosome pathway
Recruitment of mitotic centrosome proteins and complexes pathway
Signaling by FGFR1 fusion mutants pathway
Signaling by FGFR mutants pathway
Signaling by FGFR in disease pathway
Signaling by FGFR1 mutants pathway
Cell Cycle pathway
Centrosome maturation pathway
G2/M Transition pathway
Cell Cycle, Mitotic pathway
Mitotic G2-G2/M phases pathway
Disease pathway
KEGG
INOH
PID NCI
Cross-References
SwissProt
TrEMBL F1N1J5
UniProt Splice Variant
Entrez Gene 506246
UniGene Bt.24497
RefSeq NM_001077859
HUGO
OMIM
CCDS
HPRD
IMGT
EMBL DAAA02027516
GenPept
RNA Seq Atlas 506246