This gene encodes a member of the SLITRK protein family. Members of this family are integral membrane proteins that are characterized by two N-terminal leucine-rich repeat (LRR) domains and a C-terminal region that shares homology with trk neurotrophin receptors. This protein functions as a regulator of neurite outgrowth required for normal hearing and vision. Mutations in this gene are a cause of myopia and deafness. [provided by RefSeq, Dec 2014]
| SKU | Test Kits | Buffer | Dye Color | Order Now |
|---|---|---|---|---|
| SLITRK6-20-RE | 20 (40 μL) | 200 μL |  |
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| SLITRK6-20-OR | 20 (40 μL) | 200 μL |  |
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| SLITRK6-20-GO | 20 (40 μL) | 200 μL |  |
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| SLITRK6-20-GR | 20 (40 μL) | 200 μL |  |
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| SLITRK6-20-AQ | 20 (40 μL) | 200 μL |  |
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This gene encodes a member of the SLITRK protein family. Members of this family are integral membrane proteins that are characterized by two N-terminal leucine-rich repeat (LRR) domains and a C-terminal region that shares homology with trk neurotrophin receptors. This protein functions as a regulator of neurite outgrowth required for normal hearing and vision. Mutations in this gene are a cause of myopia and deafness. [provided by RefSeq, Dec 2014]
Gene Symbol : SLITRK6
Gene Name : SLIT and NTRK like family member 6
Chromosome : CHR 13: 857,993,47-857,927,86
Locus : 13q31.1
Alt. Genes : SGK2
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