collagen, type IV, alpha 5

Symbol

COL4A5 (may also be known as: None)

Organism

Human

Description

This gene encodes one of the six subunits of type IV collagen, the major structural component of basement membranes. Mutations in this gene are associated with X-linked Alport syndrome, also known as hereditary nephritis. Like the other members of the type IV collagen gene family, this gene is organized in a head-to-head conformation with another type IV collagen gene so that each gene pair shares a common promoter. Alternatively spliced transcript variants have been identified for this gene. [provided by RefSeq, Aug 2010]

Orthologs

SymbolSpecies
col4a5 Danio rerio
Col4a5 Mus musculus

Links to external resources

Changes associated with this gene

GO Terms

GO IDGO TermGO Category
GO:0007411 axon guidance biological_process
GO:0007528 neuromuscular junction development biological_process
GO:0005576 extracellular region cellular_component
GO:0005581 collagen cellular_component
GO:0005587 collagen type IV cellular_component
GO:0005605 basal lamina cellular_component
GO:0031594 neuromuscular junction cellular_component
GO:0005201 extracellular matrix structural constituent molecular_function
GO:0005488 binding molecular_function