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: 84984
MIM: 615586
HGNC: 28209
Ensembl: ENSG00000174007
Variants:
dbSNP: 84984
ClinVar: 84984
TCGA: ENSG00000174007
COSMIC: CEP19
RNA/Proteins
| Gene ID | Transcript ID | Uniprot |
|---|---|---|
| ENSG00000174007 | ENST00000399942 | A8MX07 |
| ENSG00000174007 | ENST00000409690 | Q96LK0 |
Expression (GTEx)
Protein levels (Protein atlas)
References
| Pubmed ID | Year | Title | Citations |
|---|---|---|---|
| 29127258 | 2018 | Homozygous mutation in CEP19, a gene mutated in morbid obesity, in Bardet-Biedl syndrome with predominant postaxial polydactyly. | 12 |
| 29127258 | 2018 | Homozygous mutation in CEP19, a gene mutated in morbid obesity, in Bardet-Biedl syndrome with predominant postaxial polydactyly. | 12 |
| 28428259 | 2017 | RABL2 interacts with the intraflagellar transport-B complex and CEP19 and participates in ciliary assembly. | 48 |
| 28625565 | 2017 | The CEP19-RABL2 GTPase Complex Binds IFT-B to Initiate Intraflagellar Transport at the Ciliary Base. | 61 |
| 28428259 | 2017 | RABL2 interacts with the intraflagellar transport-B complex and CEP19 and participates in ciliary assembly. | 48 |
| 28625565 | 2017 | The CEP19-RABL2 GTPase Complex Binds IFT-B to Initiate Intraflagellar Transport at the Ciliary Base. | 61 |
| 24268657 | 2013 | Morbid obesity resulting from inactivation of the ciliary protein CEP19 in humans and mice. | 34 |
| 24268657 | 2013 | Morbid obesity resulting from inactivation of the ciliary protein CEP19 in humans and mice. | 34 |
Citation
Dessen P
CEP19 (centrosomal protein 19)
Atlas Genet Cytogenet Oncol Haematol. 2014-11-01
Online version: http://atlasgeneticsoncology.org/gene/61721/cep19-(centrosomal-protein-19)
