SCUBA

NUP62 — Nucleoporin 62

NUP62 belongs to a gene co-expression module in 5 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.

NUP62's module in each cell type

Cell typeModuleShares the module with
CD4⁺ T cellsEffector activation NFkB
TCR/AP1/NFKb pathway
ADAM19, AHR, ARFGAP3, ATF5, BHLHE40, CGAS, DUSP5, ETF1 +23 moreView in SCUBA
Gamma-delta T cellsEOMES Effector Program
T cell maturation
AGK, ANKZF1, ATG16L2, C6orf120, CARD8, CBX1, CDK5RAP3, CENPT +25 more
Innate lymphoid cellsRNA Chromatin Regulation
RNA processing & translation
ACADM, AURKAIP1, BUD23, CBX3, CMC2, COPB1, DNAJA2, DYNC1LI1 +19 moreView in SCUBA
MacrophagesNuclear Pore Transport
Housekeeping
AARS1, APH1A, ARF3, ATG3, CNOT7, CTDNEP1, DCAF7, GNAI2 +18 moreView in SCUBA
Mucosal-associated invariant T cellOxidative Stress Response
Stress
ATIC, CD244, CYTH4, EIF2S2, GPR68, GSDMD, ING4, KEAP1 +11 more

About the gene

SynonymsDKFZp547L134, FLJ20822, FLJ43869, IBSN, MGC841, p62, SNDI
Chromosome19: 49906825-49929764
Predicted locationIntracellular
Essential geneYes
Protein classDisease related genes, Essential proteins, Human disease related genes, Metabolic proteins, Potential drug targets, Predicted intracellular proteins, Transporters
Biological processHost-virus interaction, mRNA transport, Protein transport, Translocation, Transport

Function

Essential component of the nuclear pore complex. The N-terminal is probably involved in nucleocytoplasmic transport. The C-terminal is involved in protein-protein interaction probably via coiled-coil formation, promotes its association with centrosomes and may function in anchorage of p62 to the pore complex. Plays a role in mitotic cell cycle progression by regulating centrosome segregation, centriole maturation and spindle orientation. It might be involved in protein recruitment to the centrosome after nuclear breakdown.

Human Protein Atlas · Open Targets · UniProt

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