This gene encodes a putative sodium-dependent amino-acid/proton antiporter. The protein has eleven transmembrane domains, an extracellular N-terminus and an intracellular C-terminal tail. The protein is a member of the SLC38 sodium-coupled neutral amino acid transporter family of proteins. Mutations in this gene result in foveal hypoplasia with or without optic nerve misrouting and/or anterior segment dysgenesis. [provided by RefSeq, May 2014]
SKU | Test Kits | Buffer | Dye Color | Order Now |
---|---|---|---|---|
SLC38A8-20-RE | 20 (40 μL) | 200 μL | Request Pricing | |
SLC38A8-20-OR | 20 (40 μL) | 200 μL | Request Pricing | |
SLC38A8-20-GO | 20 (40 μL) | 200 μL | Request Pricing | |
SLC38A8-20-GR | 20 (40 μL) | 200 μL | Request Pricing | |
SLC38A8-20-AQ | 20 (40 μL) | 200 μL | Request Pricing |
This gene encodes a putative sodium-dependent amino-acid/proton antiporter. The protein has eleven transmembrane domains, an extracellular N-terminus and an intracellular C-terminal tail. The protein is a member of the SLC38 sodium-coupled neutral amino acid transporter family of proteins. Mutations in this gene result in foveal hypoplasia with or without optic nerve misrouting and/or anterior segment dysgenesis. [provided by RefSeq, May 2014]
Gene Symbol : SLC38A8
Gene Name : Solute carrier family 38 member 8
Chromosome : CHR 16: 840,433,71-840,096,66
Locus : 16q23.3
Alt. Genes : CLEC3A
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