SCUBA

FAM107A — Family with sequence similarity 107 member A

FAM107A belongs to a gene co-expression module in 3 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.

FAM107A's module in each cell type

Cell typeModuleShares the module with
EndothelialEC Quiescence Identity
Endothelial cell development
ABCC4, ARHGAP5, C1orf115, ENPP4, GIT2, IFNAR2, LRRFIP1, MSI2 +8 moreView in SCUBA
FibroblastsSubepithelial Fibroblast Identity
Developmental
ANGPTL1, APBB1IP, ARHGAP15, CNTN1, CP, ECM2, EFEMP1, FGF13 +12 moreView in SCUBA
PericytesVascular Barrier Integrity
Migration & adhesion
C1orf115, GIMAP1, GIMAP4, GIMAP7, ITGB4, JAM2, MYCT1, NRN1 +2 moreView in SCUBA

About the gene

SynonymsDRR1, TU3A
Chromosome3: 58564117-58627610
Predicted locationIntracellular
Essential geneNo
Protein classPredicted intracellular proteins
Molecular functionActin-binding
Biological processCell cycle, Growth regulation, Stress response

Function

Stress-inducible actin-binding protein that plays a role in synaptic and cognitive functions by modulating actin filamentous (F- actin) dynamics. Mediates polymerization of globular actin to F-actin. Also binds to, stabilizes and bundles F-actin. Involved in synaptic function by regulating neurite outgrowth in an actin-dependent manner and for the acquisition of hippocampus-dependent cognitive function, such as learning and long-term memory (By similarity). Plays a role in the actin and microtubule cytoskeleton organization; negatively regulates focal adhesion (FA) assembly promoting malignant glial cell migration in an actin-, microtubule- and MAP1A-dependent manner. Also involved in neuroblastoma G1/S phase cell cycle progression and cell proliferation inhibition by stimulating ubiquitination of NF-kappa-B subunit RELA and NF-kappa-B degradation in a COMMD1- and actin-dependent manner. May play a role in tumor development.

Human Protein Atlas · Open Targets · UniProt

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