SCUBA

CCDC88C — Coiled-coil domain containing 88C

CCDC88C 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.

CCDC88C's module in each cell type

Cell typeModuleShares the module with
CD4⁺ T cellsDNA repair/replication
DNA/chromatin regulation
ACAP2, BROX, CKAP2, EPM2AIP1, FOXO3, HAUS3, HELB, KMT2C +4 moreView in SCUBA
EndothelialArterial EC Identity
Endothelial cell development
ABR, AIF1L, ASS1, CPNE8, EPHA4, IFITM2, MOB2, RAB30 +5 moreView in SCUBA
Gamma-delta T cellsTCR-Cytokine Signaling
TCR Signaling
ARHGAP26, CACNA2D2, LPGAT1, LY75, MED15, NBPF14, NBPF19, NBPF20 +10 more
Mucosal-associated invariant T cellTCR Activation Signaling
TCR Signaling
ARFGEF1, ARIH1, CARD11, CD226, GLS, KANSL1, KMT5B, MAP3K2 +12 more

About the gene

SynonymsDAPLE, HkRP2, KIAA1509, SCA40
Chromosome14: 91271323-91417844
Predicted locationIntracellular
Essential geneNo
Protein classDisease related genes, Human disease related genes, Plasma proteins, Predicted intracellular proteins
Molecular functionGuanine-nucleotide releasing factor
Biological processWnt signaling pathway

Function

Required for activation of guanine nucleotide-binding proteins (G-proteins) during non-canonical Wnt signaling. Binds to ligand-activated Wnt receptor FZD7, displacing DVL1 from the FZD7 receptor and leading to inhibition of canonical Wnt signaling. Acts as a non-receptor guanine nucleotide exchange factor by also binding to guanine nucleotide-binding protein G(i) alpha (Gi-alpha) subunits, leading to their activation. Binding to Gi-alpha subunits displaces the beta and gamma subunits from the heterotrimeric G-protein complex, triggering non-canonical Wnt responses such as activation of RAC1 and PI3K-AKT signaling. Promotes apical constriction of cells via ARHGEF18

Human Protein Atlas · Open Targets · UniProt

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