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: 9662
MIM: 611423
HGNC: 29086
Ensembl: ENSG00000174799
Variants:
dbSNP: 9662
ClinVar: 9662
TCGA: ENSG00000174799
COSMIC: CEP135
RNA/Proteins
| Gene ID | Transcript ID | Uniprot |
|---|---|---|
| ENSG00000174799 | ENST00000257287 | Q66GS9 |
| ENSG00000174799 | ENST00000422247 | Q66GS9 |
Expression (GTEx)
Pathways
References
| Pubmed ID | Year | Title | Citations |
|---|---|---|---|
| 38062802 | 2023 | Centrosomal Protein CEP135 Regulates the Migration and Angiogenesis of Endothelial Cells in a Microtubule-Dependent Manner. | 0 |
| 38062802 | 2023 | Centrosomal Protein CEP135 Regulates the Migration and Angiogenesis of Endothelial Cells in a Microtubule-Dependent Manner. | 0 |
| 35406752 | 2022 | Mitotic Maturation Compensates for Premature Centrosome Splitting and PCM Loss in Human cep135 Knockout Cells. | 2 |
| 35406752 | 2022 | Mitotic Maturation Compensates for Premature Centrosome Splitting and PCM Loss in Human cep135 Knockout Cells. | 2 |
| 32643282 | 2020 | Mutation in CEP135 causing primary microcephaly and subcortical heterotopia. | 4 |
| 32643282 | 2020 | Mutation in CEP135 causing primary microcephaly and subcortical heterotopia. | 4 |
| 30811267 | 2019 | CEP135 isoform dysregulation promotes centrosome amplification in breast cancer cells. | 15 |
| 30811267 | 2019 | CEP135 isoform dysregulation promotes centrosome amplification in breast cancer cells. | 15 |
| 30531682 | 2018 | The Association of CEP135 rs4865047 and NPY2R rs1902491 Single Nucleotide Polymorphisms (SNPs) with Rapid Progression of Proliferative Diabetic Retinopathy in Patients with Type 1 Diabetes Mellitus. | 3 |
| 30531682 | 2018 | The Association of CEP135 rs4865047 and NPY2R rs1902491 Single Nucleotide Polymorphisms (SNPs) with Rapid Progression of Proliferative Diabetic Retinopathy in Patients with Type 1 Diabetes Mellitus. | 3 |
| 26657937 | 2016 | A novel splice site mutation in CEP135 is associated with primary microcephaly in a Pakistani family. | 10 |
| 27477386 | 2016 | The Human Centriolar Protein CEP135 Contains a Two-Stranded Coiled-Coil Domain Critical for Microtubule Binding. | 17 |
| 26657937 | 2016 | A novel splice site mutation in CEP135 is associated with primary microcephaly in a Pakistani family. | 10 |
| 27477386 | 2016 | The Human Centriolar Protein CEP135 Contains a Two-Stranded Coiled-Coil Domain Critical for Microtubule Binding. | 17 |
| 26412126 | 2015 | A Short CEP135 Splice Isoform Controls Centriole Duplication. | 9 |
Citation
Dessen P
CEP135 (centrosomal protein 135)
Atlas Genet Cytogenet Oncol Haematol. 2021-06-01
Online version: http://atlasgeneticsoncology.org/gene/58365/cep135-(centrosomal-protein-135)
