The protein encoded by this gene is a GTPase and a Golgi body transmembrane protein. The encoded protein can form a homotetramer and has been shown to interact with spastin and with mitogen-activated protein kinase kinase kinase kinase 4. This protein may be involved in axonal maintenance as evidenced by the fact that defects in this gene are a cause of spastic paraplegia type 3. Three transcript variants encoding two different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]
SKU | Test Kits | Buffer | Dye Color | Order Now |
---|---|---|---|---|
ATL1-20-RE | 20 (40 μL) | 200 μL | Request Pricing | |
ATL1-20-OR | 20 (40 μL) | 200 μL | Request Pricing | |
ATL1-20-GO | 20 (40 μL) | 200 μL | Request Pricing | |
ATL1-20-GR | 20 (40 μL) | 200 μL | Request Pricing | |
ATL1-20-AQ | 20 (40 μL) | 200 μL | Request Pricing |
The protein encoded by this gene is a GTPase and a Golgi body transmembrane protein. The encoded protein can form a homotetramer and has been shown to interact with spastin and with mitogen-activated protein kinase kinase kinase kinase 4. This protein may be involved in axonal maintenance as evidenced by the fact that defects in this gene are a cause of spastic paraplegia type 3. Three transcript variants encoding two different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]
Gene Symbol : ATL1
Gene Name : Atlastin GTPase 1
Chromosome : CHR 14: 505,330,81-506,330,67
Locus : 14q22.1
Alt. Genes : LRPPRC
Lorem Ipsum is simply dummy text of the printing and typesetting industry.
Lorem Ipsum is simply dummy text of the printing and typesetting industry.