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: 92002
MIM: 300708
HGNC: 28434
Ensembl: ENSG00000262919
Variants:
dbSNP: 92002
ClinVar: 92002
TCGA: ENSG00000262919
COSMIC: CCNQ
RNA/Proteins
Protein levels (Protein atlas)
References
| Pubmed ID | Year | Title | Citations |
|---|---|---|---|
| 35291876 | 2022 | Functional characterization of the human Cdk10/Cyclin Q complex. | 7 |
| 35291876 | 2022 | Functional characterization of the human Cdk10/Cyclin Q complex. | 7 |
| 34369103 | 2021 | Functional characterization of CDK10 and cyclin M truncated variants causing severe developmental disorders. | 1 |
| 34369103 | 2021 | Functional characterization of CDK10 and cyclin M truncated variants causing severe developmental disorders. | 1 |
| 28322501 | 2017 | Multigenerational pedigree with STAR syndrome: A novel FAM58A variant and expansion of the phenotype. | 7 |
| 28322501 | 2017 | Multigenerational pedigree with STAR syndrome: A novel FAM58A variant and expansion of the phenotype. | 7 |
| 26882209 | 2016 | Ocular manifestations of X-linked dominant FAM58A mutation in toe syndactyly, telecanthus, anogenital, and renal malformations ('STAR') syndrome. | 5 |
| 26882209 | 2016 | Ocular manifestations of X-linked dominant FAM58A mutation in toe syndactyly, telecanthus, anogenital, and renal malformations ('STAR') syndrome. | 5 |
| 18297069 | 2008 | Mutations in the cyclin family member FAM58A cause an X-linked dominant disorder characterized by syndactyly, telecanthus and anogenital and renal malformations. | 20 |
| 18297069 | 2008 | Mutations in the cyclin family member FAM58A cause an X-linked dominant disorder characterized by syndactyly, telecanthus and anogenital and renal malformations. | 20 |
Citation
Dessen P
CCNQ (cyclin Q)
Atlas Genet Cytogenet Oncol Haematol. 2017-09-01
Online version: http://atlasgeneticsoncology.org/gene/79048/ccnq-(cyclin-q)
