CDK10 (cyclin dependent kinase 10)

2003-12-01  

Identity

HGNC
LOCATION
16q24.3
LOCUSID
ALIAS
ALSAS,PISSLRE
FUSION GENES

Other Information

Locus ID:

NCBI: 8558
MIM: 603464
HGNC: 1770
Ensembl: ENSG00000185324

Variants:

dbSNP: 8558
ClinVar: 8558
TCGA: ENSG00000185324
COSMIC: CDK10

RNA/Proteins

Gene IDTranscript IDUniprot
ENSG00000185324ENST00000331006F8W872
ENSG00000185324ENST00000353379Q15131
ENSG00000185324ENST00000502547D6REZ2
ENSG00000185324ENST00000505473Q15131
ENSG00000185324ENST00000508723D6RA59
ENSG00000185324ENST00000510811Q9UHL7
ENSG00000185324ENST00000511415D6RHH3
ENSG00000185324ENST00000512912D6REZ2
ENSG00000185324ENST00000564192H3BT74
ENSG00000185324ENST00000565470H3BSN8
ENSG00000185324ENST00000617879Q15131
ENSG00000185324ENST00000625631Q9UHL7

Expression (GTEx)

0
10
20
30
40
50
60
70
80
90

Protein levels (Protein atlas)

Not detected
Low
Medium
High

References

Pubmed IDYearTitleCitations
377374532024CDK10 suppresses metastasis of lung adenocarcinoma through inhibition of the ETS2/c-Raf/p-MEK/p-ERK signaling loop.1
383766062024RNF115 aggravates tumor progression through regulation of CDK10 degradation in thyroid carcinoma.1
377374532024CDK10 suppresses metastasis of lung adenocarcinoma through inhibition of the ETS2/c-Raf/p-MEK/p-ERK signaling loop.1
383766062024RNF115 aggravates tumor progression through regulation of CDK10 degradation in thyroid carcinoma.1
365039222023A sib-pair with Al Kaissi syndrome caused by homozygosity for a novel CDK10 splice variant.1
369887712023CDK10, CDK11, FOXO1, and FOXO3 Gene Expression in Alzheimer's Disease Encephalic Samples.1
365039222023A sib-pair with Al Kaissi syndrome caused by homozygosity for a novel CDK10 splice variant.1
369887712023CDK10, CDK11, FOXO1, and FOXO3 Gene Expression in Alzheimer's Disease Encephalic Samples.1
352918762022Functional characterization of the human Cdk10/Cyclin Q complex.7
352918762022Functional characterization of the human Cdk10/Cyclin Q complex.7
343691032021Functional characterization of CDK10 and cyclin M truncated variants causing severe developmental disorders.1
347374402021A large Canadian cohort provides insights into the genetic architecture of human hair colour.7
343691032021Functional characterization of CDK10 and cyclin M truncated variants causing severe developmental disorders.1
347374402021A large Canadian cohort provides insights into the genetic architecture of human hair colour.7
323459882020Gene expression network analysis of lymph node involvement in colon cancer identifies AHSA2, CDK10, and CWC22 as possible prognostic markers.5

Citation

Dessen P

CDK10 (cyclin dependent kinase 10)

Atlas Genet Cytogenet Oncol Haematol. 2003-12-01

Online version: http://atlasgeneticsoncology.org/gene/40030/deep-insight-explorer/deep-insight-explorer/case-report-explorer/