SCUBA

CLSPN — Claspin

CLSPN belongs to a gene co-expression module in 6 of 28 SCUBA cell types. Each module groups genes that rise and fall together in that cell type; the genes it shares a module with are its closest co-expression partners there.

CLSPN's module in each cell type

Cell typeModuleShares the module with
CD19⁺ B cellsReplication Licensing
Cell cycle
ASF1B, CDC6, CDCA5, CDT1, CENPK, CENPU, DNAJC9, FAM111B +5 moreView in SCUBA
Gamma-delta T cellsS-phase Replication
Cell cycle
ATAD2, ATAD5, BRCA2, CDT1, CENPH, CENPM, CENPU, DHFR +13 more
Goblet cellsReplication Fork Checkpoint
Cell cycle
ATAD2, BRCA2, CENPM, DNAJC9, FANCI, LIG1, PKMYT1, RRM1View in SCUBA
Hematopoietic progenitor cellsReplication Origin Licensing
Cell cycle
BRCA1, CDC6, DTL, FAM111B, MCM10, ORC6, WDR76, XRCC2
MacrophagesS-phase DNA Replication
Cell cycle
ATAD2, ATAD5, BARD1, BRCA1, CENPK, CENPM, CENPU, DHFR +31 moreView in SCUBA
Natural Killer cellsS-phase Replication
Cell cycle
CDT1, CENPM, CENPU, FANCI, PCLAF, RRM2, TYMSView in SCUBA

About the gene

Chromosome1: 35720218-35769978
Predicted locationIntracellular
Essential geneYes
Protein classEssential proteins, Predicted intracellular proteins
Molecular functionDNA-binding
Biological processCell cycle, DNA damage, DNA repair

Function

Required for checkpoint mediated cell cycle arrest in response to inhibition of DNA replication or to DNA damage induced by both ionizing and UV irradiation. Adapter protein which binds to BRCA1 and the checkpoint kinase CHEK1 and facilitates the ATR-dependent phosphorylation of both proteins. Also required to maintain normal rates of replication fork progression during unperturbed DNA replication. Binds directly to DNA, with particular affinity for branched or forked molecules and interacts with multiple protein components of the replisome such as the MCM2-7 complex and TIMELESS. Important for initiation of DNA replication, recruits kinase CDC7 to phosphorylate MCM2-7 components.

Human Protein Atlas · Open Targets · UniProt

Gene annotation from the Human Protein Atlas and UniProt; see sources & licences.