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
Symbol | Species | |
---|---|---|
col4a5 | Danio rerio | |
Col4a5 | Mus musculus |
Links to external resources
Changes associated with this gene
GO Terms
GO ID | GO Term | GO 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 | |