The protein encoded by this gene is a sodium-dependent neutral amino acid transporter for alanine, serine, cysteine, and threonine. Defects in this gene have been associated with developmental delay, microcephaly, and intellectual disability. [provided by RefSeq, Jan 2017]
| SKU | Test Kits | Buffer | Dye Color | Order Now |
|---|---|---|---|---|
| SLC1A4-20-RE | 20 (40 μL) | 200 μL |  |
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| SLC1A4-20-OR | 20 (40 μL) | 200 μL |  |
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| SLC1A4-20-GO | 20 (40 μL) | 200 μL |  |
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| SLC1A4-20-GR | 20 (40 μL) | 200 μL |  |
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| SLC1A4-20-AQ | 20 (40 μL) | 200 μL |  |
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The protein encoded by this gene is a sodium-dependent neutral amino acid transporter for alanine, serine, cysteine, and threonine. Defects in this gene have been associated with developmental delay, microcephaly, and intellectual disability. [provided by RefSeq, Jan 2017]
Gene Symbol : SLC1A4
Gene Name : Solute carrier family 1 member 4
Chromosome : CHR 2: 649,884,44-650,238,64
Locus : 2p14
Alt. Genes : ENAM
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