background:
SLC23A3 (Solute Carrier Family 23, Member 3) is a Protein Coding gene. Diseases associated with SLC23A3 include epilepsy, generalized, with febrile seizures plus, type 5. GO annotations related to this gene include transporter activity. An important paralog of this gene is SLC23A1.
Subcellular Location:
Membrane.
Similarity:
Belongs to the xanthine/uracil permease family. Nucleobase:cation symporter-2 (NCS2) (TC 2.A.40) subfamily.
Database links:
Entrez Gene: 151295 Human
Entrez Gene: 22626 Mouse
Entrez Gene: 367298 Rat
SwissProt: Q6PIS1 Human
SwissProt: Q60850 Mouse
Unigene: 124565 Human
Unigene: 68157 Mouse
Important Note:
This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.
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