The protein encoded by this gene is a highly hydrophobic integral membrane protein belonging to the MAL family of proteolipids. The protein has been localized to the endoplasmic reticulum of T-cells and is a candidate linker protein in T-cell signal transduction. In addition, this proteolipid is localized in compact myelin of cells in the nervous system and has been implicated in myelin biogenesis and/or function. The protein plays a role in the formation, stabilization and maintenance of glycosphingolipid-enriched membrane microdomains. Down-regulation of this gene has been associated with a variety of human epithelial malignancies. Alternative splicing produces four transcript variants which vary from each other by the presence or absence of alternatively spliced exons 2 and 3. [provided by RefSeq, May 2012]
SKU | Test Kits | Buffer | Dye Color | Order Now |
---|---|---|---|---|
MAL-20-RE | 20 (40 μL) | 200 μL | Request Pricing | |
MAL-20-OR | 20 (40 μL) | 200 μL | Request Pricing | |
MAL-20-GO | 20 (40 μL) | 200 μL | Request Pricing | |
MAL-20-GR | 20 (40 μL) | 200 μL | Request Pricing | |
MAL-20-AQ | 20 (40 μL) | 200 μL | Request Pricing |
The protein encoded by this gene is a highly hydrophobic integral membrane protein belonging to the MAL family of proteolipids. The protein has been localized to the endoplasmic reticulum of T-cells and is a candidate linker protein in T-cell signal transduction. In addition, this proteolipid is localized in compact myelin of cells in the nervous system and has been implicated in myelin biogenesis and/or function. The protein plays a role in the formation, stabilization and maintenance of glycosphingolipid-enriched membrane microdomains. Down-regulation of this gene has been associated with a variety of human epithelial malignancies. Alternative splicing produces four transcript variants which vary from each other by the presence or absence of alternatively spliced exons 2 and 3. [provided by RefSeq, May 2012]
Gene Symbol : MAL
Gene Name : Mal, T-cell differentiation protein
Chromosome : CHR 2: 950,256,54-950,539,91
Locus : 2q11.1
Alt. Genes : RBM12
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