SCUBA

HECTD1 — HECT domain E3 ubiquitin protein ligase 1

HECTD1 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.

HECTD1's module in each cell type

Cell typeModuleShares the module with
CD4⁺ T cellsDNA damage response
DNA/chromatin regulation
ATP2B1, CENPC, DEAF1, FBXO34, HAX1, KMT5C, MRPL50, NDUFA5 +7 moreView in SCUBA
Gamma-delta T cellsWnt-STAT3 Signaling
TCR Signaling
BTBD1, COPA, CTNNB1, DHX9, EZR, NUP153, PAFAH1B1, SPRTN +5 more
Innate lymphoid cellsNK ILC Tissue Homing
Homing & TEM
ADGRE5, AKAP13, AREG, ARL4C, ATP1B3, B3GNT7, BTG1, CCDC107 +25 moreView in SCUBA
MacrophagesTranscriptional Repression
Housekeeping
AKAP8, ANKRD11, ARIH2, BACH1, CCNT2, CDK13, CEP95, CSNK1D +23 moreView in SCUBA
MonocytesGlucocorticoid Transcription
Inflammatory
JDP2, KLF13, KLF9, PER1, PIK3R1, TMEM123, ZBTB16View in SCUBA

About the gene

SynonymsKIAA1131
Chromosome14: 31100117-31207804
Predicted locationIntracellular
Essential geneNo
Protein classEnzymes, Metabolic proteins, Predicted intracellular proteins
Molecular functionTransferase
Biological processUbl conjugation pathway

Function

E3 ubiquitin-protein ligase which accepts ubiquitin from an E2 ubiquitin-conjugating enzyme in the form of a thioester and then directly transfers the ubiquitin to targeted substrates. Mediates 'Lys-63'-linked polyubiquitination of HSP90AA1 which leads to its intracellular localization and reduced secretion (By similarity). Negatively regulating HSP90AA1 secretion in cranial mesenchyme cells may impair their emigration and may be essential for the correct development of the cranial neural folds and neural tube closure (By similarity). Catalyzes ubiquitination and degradation of ZNF622, an assembly factor for the ribosomal 60S subunit, in hematopoietic cells, thereby promoting hematopoietic stem cell renewal.

Human Protein Atlas · Open Targets · UniProt

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