This gene belongs to a small gene family whose members have an N-terminal VHS domain followed by a GAT domain; domains which typically participate in vesicular trafficking. The canonical protein encoded by this gene also has a C-terminal clathrin binding motif. This protein has been shown to interact with Tollip, clathrin and ubiquitin and is thought to play a role in endosomal sorting. This gene resides in the 3.7 Mb deletion of chromosome region 17p11.2 that is associated with Smith-Magenis syndrome. Alternative splicing results in multiple transcript variants encoding distinct proteins. [provided by RefSeq, Apr 2017]
| SKU | Test Kits | Buffer | Dye Color | Order Now |
|---|---|---|---|---|
| TOM1L2-20-RE | 20 (40 μL) | 200 μL |  |
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| TOM1L2-20-OR | 20 (40 μL) | 200 μL |  |
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| TOM1L2-20-GO | 20 (40 μL) | 200 μL |  |
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| TOM1L2-20-GR | 20 (40 μL) | 200 μL |  |
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| TOM1L2-20-AQ | 20 (40 μL) | 200 μL |  |
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This gene belongs to a small gene family whose members have an N-terminal VHS domain followed by a GAT domain; domains which typically participate in vesicular trafficking. The canonical protein encoded by this gene also has a C-terminal clathrin binding motif. This protein has been shown to interact with Tollip, clathrin and ubiquitin and is thought to play a role in endosomal sorting. This gene resides in the 3.7 Mb deletion of chromosome region 17p11.2 that is associated with Smith-Magenis syndrome. Alternative splicing results in multiple transcript variants encoding distinct proteins. [provided by RefSeq, Apr 2017]
Gene Symbol : TOM1L2
Gene Name : Target of myb1 like 2 membrane trafficking protein
Chromosome : CHR 17: 179,724,69-178,435,07
Locus : 17p11.2
Alt. Genes : FEM1B
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