Non-annotated gene. Preliminary data : if you are an author who wish to write a full paper/card on this gene, contribute in submission tool
Other Information
Locus ID:
NCBI: 26128
MIM: 609367
HGNC: 23419
Ensembl: ENSG00000198954
Variants:
dbSNP: 26128
ClinVar: 26128
TCGA: ENSG00000198954
COSMIC: KIFBP
RNA/Proteins
References
| Pubmed ID | Year | Title | Citations |
|---|---|---|---|
| 37903629 | 2024 | Progressive ataxia, ophthalmoparesis, and hypogonadotropic hypogonadism in a family with a novel variant in the KIFBP gene. | 0 |
| 37903629 | 2024 | Progressive ataxia, ophthalmoparesis, and hypogonadotropic hypogonadism in a family with a novel variant in the KIFBP gene. | 0 |
| 32939943 | 2020 | Goldberg-Shprintzen syndrome is determined by the absence, or reduced expression levels, of KIFBP. | 4 |
| 33252036 | 2020 | The mechanism of kinesin inhibition by kinesin-binding protein. | 13 |
| 32939943 | 2020 | Goldberg-Shprintzen syndrome is determined by the absence, or reduced expression levels, of KIFBP. | 4 |
| 33252036 | 2020 | The mechanism of kinesin inhibition by kinesin-binding protein. | 13 |
| 30709852 | 2019 | Kinesin-binding protein ensures accurate chromosome segregation by buffering KIF18A and KIF15. | 11 |
| 30709852 | 2019 | Kinesin-binding protein ensures accurate chromosome segregation by buffering KIF18A and KIF15. | 11 |
| 28445502 | 2017 | Role of Kif15 and its novel mitotic partner KBP in K-fiber dynamics and chromosome alignment. | 12 |
| 28445502 | 2017 | Role of Kif15 and its novel mitotic partner KBP in K-fiber dynamics and chromosome alignment. | 12 |
| 26948876 | 2016 | Kinesin-Binding Protein Controls Microtubule Dynamics and Cargo Trafficking by Regulating Kinesin Motor Activity. | 57 |
| 26948876 | 2016 | Kinesin-Binding Protein Controls Microtubule Dynamics and Cargo Trafficking by Regulating Kinesin Motor Activity. | 57 |
| 23427148 | 2013 | KBP-cytoskeleton interactions underlie developmental anomalies in Goldberg-Shprintzen syndrome. | 15 |
| 24072599 | 2013 | Homozygous truncating mutation of the KBP gene, encoding a KIF1B-binding protein, in a familial case of fetal polymicrogyria. | 15 |
| 23427148 | 2013 | KBP-cytoskeleton interactions underlie developmental anomalies in Goldberg-Shprintzen syndrome. | 15 |
Citation
Dessen P
KIFBP (kinesin family binding protein)
Atlas Genet Cytogenet Oncol Haematol. 2014-11-01
Online version: http://atlasgeneticsoncology.org/gene/64880/kifbp-(kinesin-family-binding-protein)
