This gene encodes a member of the inwardly rectifying potassium channel family of proteins. Members of this family form ion channel pores that allow potassium ions to pass into a cell. The encoded protein belongs to a subfamily of low signal channel conductance proteins that have a low dependence on potassium concentration. Mutations in this gene are associated with snowflake vitreoretinal degeneration. Alternate splicing results in multiple transcript variants.[provided by RefSeq, Feb 2010]
| SKU | Test Kits | Buffer | Dye Color | Order Now |
|---|---|---|---|---|
| KCNJ13-20-RE | 20 (40 μL) | 200 μL |  |
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| KCNJ13-20-OR | 20 (40 μL) | 200 μL |  |
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| KCNJ13-20-GO | 20 (40 μL) | 200 μL |  |
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| KCNJ13-20-GR | 20 (40 μL) | 200 μL |  |
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| KCNJ13-20-AQ | 20 (40 μL) | 200 μL |  |
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This gene encodes a member of the inwardly rectifying potassium channel family of proteins. Members of this family form ion channel pores that allow potassium ions to pass into a cell. The encoded protein belongs to a subfamily of low signal channel conductance proteins that have a low dependence on potassium concentration. Mutations in this gene are associated with snowflake vitreoretinal degeneration. Alternate splicing results in multiple transcript variants.[provided by RefSeq, Feb 2010]
Gene Symbol : KCNJ13
Gene Name : Potassium voltage-gated channel subfamily J member 13
Chromosome : CHR 2: 232,776,564-232,765,801
Locus : 2q37.1
Alt. Genes : TRAP1
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