SCUBA

UBD — Ubiquitin D

UBD belongs to a gene co-expression module in 4 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.

UBD's module in each cell type

Cell typeModuleShares the module with
EndothelialIFN-gamma Response
Inflammation
APOL2, APOL6, BATF2, CARD16, CASP1, CD40, CXCL10, CXCL11 +18 moreView in SCUBA
FibroblastsNF-κB Inflammatory Activation
Inflammatory
BIRC3, CD40, CTSS, DRAM1, HAPLN3, IL15RA, IL32, LAP3 +5 moreView in SCUBA
Glial cellsNF-κB/IFN Inflammatory
Inflammation
BIRC3, CTSS, CXCL10, CXCL2, CXCL9, FDCSP, HAPLN3, ICAM1 +4 moreView in SCUBA
MacrophagesInflammasome Pyroptosis
Inflammatory
ARRDC1, ATOX1, CSTA, EMP2, ENPP2, FBXO6, GSDMD, HLA-DQB2 +12 moreView in SCUBA

About the gene

SynonymsFAT10
Chromosome6: 29555515-29559732
Predicted locationIntracellular
Essential geneNo
Protein classPredicted intracellular proteins
Biological processUbl conjugation pathway

Function

Ubiquitin-like protein modifier which can be covalently attached to target proteins and subsequently leads to their degradation by the 26S proteasome, in a NUB1-dependent manner. Conjugation to the target protein is activated by UBA6 via adenylation of its C-terminal glycine. Promotes the expression of the proteasome subunit beta type-9 (PSMB9/LMP2). Regulates TNF-alpha- induced and LPS-mediated activation of the central mediator of innate immunity NF-kappa-B by promoting TNF-alpha-mediated proteasomal degradation of ubiquitinated-I-kappa-B-alpha. Required for TNF-alpha-induced p65 nuclear translocation in renal tubular epithelial cells (RTECs). May be involved in dendritic cell (DC) maturation, the process by which immature dendritic cells differentiate into fully competent antigen-presenting cells that initiate T-cell responses. Mediates mitotic non- disjunction and chromosome instability, in long-term in vitro culture and cancers, by abbreviating mitotic phase and impairing the kinetochore localization of MAD2L1 during the prometaphase stage of the cell cycle. May be involved in the formation of aggresomes when proteasome is saturated or impaired. Mediates apoptosis in a caspase-dependent manner, especially in renal epithelium and tubular cells during renal diseases such as polycystic kidney disease and Human immunodeficiency virus (HIV)-associated nephropathy (HIVAN).

Human Protein Atlas · Open Targets · UniProt

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