SCUBA

DAG1 — Dystroglycan 1

DAG1 belongs to a gene co-expression module in 2 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.

DAG1's module in each cell type

Cell typeModuleShares the module with
EndothelialIntegrin-Actin Adhesion
migration & adhesion
APP, CHD3, CTNNA1, DOCK6, FKBP9, FMNL3, ITGA9, ITGB1 +6 moreView in SCUBA
Glial cellsGlial Adhesion Identity
migration & adhesion
ADAM23, CADM4, CALU, HMCN1, HMGN1, ITGA2, PTPRZ1, SDC3 +2 moreView in SCUBA

About the gene

Synonyms156DAG, A3a, AGRNR, DAG
Chromosome3: 49468713-49535618
Predicted locationMembrane
Essential geneNo
Protein classDisease related genes, Human disease related genes, Plasma proteins, Potential drug targets, Predicted membrane proteins, Transporters
Molecular functionHost cell receptor for virus entry, Receptor
Biological processHost-virus interaction

Function

The dystroglycan complex is involved in a number of processes including laminin and basement membrane assembly, sarcolemmal stability, cell survival, peripheral nerve myelination, nodal structure, cell migration, and epithelial polarization. Extracellular peripheral glycoprotein that acts as a receptor for extracellular matrix proteins containing laminin-G domains. Receptor for laminin-2 (LAMA2) and agrin in peripheral nerve Schwann cells. Also acts as a receptor for laminin LAMA5 (By similarity). Transmembrane protein that plays important roles in connecting the extracellular matrix to the cytoskeleton. Acts as a cell adhesion receptor in both muscle and non- muscle tissues. Receptor for both DMD and UTRN and, through these interactions, scaffolds axin to the cytoskeleton. Also functions in cell adhesion-mediated signaling and implicated in cell polarity. (Microbial infection) Acts as a receptor for lassa virus and lymphocytic choriomeningitis virus glycoprotein and class C new-world arenaviruses. Acts as a Schwann cell receptor for Mycobacterium leprae, the causative organism of leprosy, but only in the presence of the G-domain of LAMA2.

Human Protein Atlas · Open Targets · UniProt

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