1. Gene
  2. CDK10 - cyclin dependent kinase 10 Gene

CDK10 - cyclin dependent kinase 10 Gene

Homo sapiens

Also known as ALSAS; PISSLRE

Gene ID: 8558 | Gene type: protein coding

About CDK10

Cytogenetic location: 16q24.3 Genomic coordinates (GRCh38): 16:89,686,689-89,696,354 (from NCBI)

This gene has 22 transcripts (splice variants), 200 orthologues, 26 paralogues and is associated with 3 phenotypes. Ubiquitous expression in duodenum (RPKM 16.8), thyroid (RPKM 15.2) and 25 other tissues.

Summary

The protein encoded by this gene belongs to the CDK subfamily of the Ser/Thr protein kinase family. The CDK subfamily members are highly similar to the gene products of S. cerevisiae cdc28, and S. pombe cdc2, and are known to be essential for cell cycle progression. This kinase has been shown to play a role in cellular proliferation and its function is limited to cell cycle G2-M phase. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, May 2009]

CDK10 Products(4)

mRNA Protein Name
NM_001098533.3 NP_001092003.2 cyclin-dependent kinase 10 isoform c
NM_001160367.2 NP_001153839.1 cyclin-dependent kinase 10 isoform d
NM_052987.4 NP_443713.2 cyclin-dependent kinase 10 isoform b
NM_052988.5 NP_443714.3 cyclin-dependent kinase 10 isoform a
Gene Ontology
  • Molecular Function
  • Biological Process
  • Cellular Component
Molecular Function GO Annotation Evidence Reference Source
enables protein binding IPI
IPI: Inferred from physical interaction
18242510 GOA
enables protein serine/threonine kinase activity IDA
IDA: Inferred from direct assay
27104747 GOA
Biological Process GO Annotation Evidence Reference Source
involved in negative regulation of cilium assembly IMP
IMP: Inferred from mutant phenotype
27104747 GOA
involved in peptidyl-threonine phosphorylation IDA
IDA: Inferred from direct assay
27104747 GOA
involved in regulation of actin cytoskeleton organization IMP
IMP: Inferred from mutant phenotype
27104747 GOA
involved in regulation of cell cycle G2/M phase transition IDA
IDA: Inferred from direct assay
7664269 GOA
Cellular Component GO Annotation Evidence Reference Source
located in ciliary basal body IDA
IDA: Inferred from direct assay
27104747 GOA
part of cyclin-dependent protein kinase holoenzyme complex IPI
IPI: Inferred from physical interaction
24218572 GOA
located in nucleus IDA
IDA: Inferred from direct assay
11006117 GOA
EXP: Inferred from Experiment IDA: Inferred from direct assay IPI: Inferred from physical interaction IMP: Inferred from mutant phenotype IGI: Inferred from genetic interaction IEP: Inferred from expression pattern

CDK10 Protein Structure

Pkinase

Pkinase: Protein kinase domain (39 - 323)

  • 0
  • 100
  • 200
  • 300
  • 360 a.a.
Protein Preferred Names Protein Names

cyclin-dependent kinase 10

CDC2-related protein kinase

Related Diseases

Diseases Alias
Al Kaissi Syndrome

ALKAS

Growth Retardation, Spine Malformation, Dysmorphic Facies, And Developmental Delay

Toe Syndactyly, Telecanthus, And Anogenital And Renal Malformations

Star Syndrome

Syndactyly-Telecanthus-Anogenital And Renal Malformations Syndrome

Syndactyly With Renal And Anogenital Malformations

STAR

Syndactyly, Telecanthus, Anogenital And Renal Malformations

Toe Syndactyly, Telecanthus, Anogenital And Renal Malformations

Acromesomelic Dysplasia 2b

Fibular Hypoplasia And Complex Brachydactyly

Du Pan Syndrome

AMD2B

Dupans

Acromesomelic Dysplasia-2b

Fibular Aplasia-Complex Brachydactyly Syndrome

Fanconi Anemia, Complementation Group A

Fanconi Anemia

Fanconi Pancytopenia

Fanconi Anemia Complementation Group A

FANCA

Fa

Fanconi Panmyelopathy

Fanconi'S Anemia

Fanconi Anaemia

Fanconi'S Anaemia

Fanconi Hypoplastic Anemia

Estren-Dameshek Variant Of Fanconi Anemia

Estren-Dameshek Variant Of Fanconi Pancytopenia

Fanconi Anemia Estren-Dameshek Variant

Fanconis Anemia

Melanoma, Cutaneous Malignant 1

Familial Melanoma

Melanoma, Cutaneous Malignant, Susceptibility To, 1

Melanoma, Malignant

CMM1

Melanoma, Cutaneous Malignant

Cmm

Familial Atypical Mole-Malignant Melanoma Syndrome

Fammm

Melanoma, Familial

Mlm

Dysplastic Nevus Syndrome, Hereditary

Dns

B-K Mole Syndrome

Melanoma, Cutaneous Malignant, 1

Malignant Melanoma, Cutaneous

Melanoma, Cutaneous, Malignant, Susceptibility To, Type 1

Dysplastic Nevus Syndrome

Cutaneous Melanoma

Familial Atypical Mole Melanoma Syndrome

Hereditary Melanoma

Diseases Alias
Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Orthologs Information

Species Symbol Source ID
Rattus norvegicus CDK10 RGD RGD:1304851
Macaca mulatta CDK10 VGNC VGNC:99499
Canis familiaris CDK10 VGNC VGNC:39043
Bos taurus CDK10 VGNC VGNC:27116
Felis catus CDK10 VGNC VGNC:60693
Mus musculus CDK10 MGD MGI:2448549
Others CDK10 NCBI