SLCO5A1
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Official Full Name
solute carrier organic anion transporter family, member 5A1 -
Overview
This gene encodes a 12 transmembrane domain protein that is a member of the solute carrier organic anion transporter superfamily. Alternative splicing results in multiple transcript variants. -
Synonyms
SLCO5A1;solute carrier organic anion transporter family, member 5A1;SLC21A15, solute carrier family 21 (organic anion transporter), member 15;solute carrier organic anion transporter family member 5A1;OATP J;OATP5A1;OATPRP4;solute carrier family 2
| Cat.# | Product name | Source (Host) | Species | Tag | Protein Length | Price |
|---|---|---|---|---|---|---|
| SLCO5A1-2998H | Recombinant Human SLCO5A1 protein, His-tagged | E.coli | Human | His | 1-128 aa |
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Involved Pathway
SLCO5A1 involved in several pathways and played different roles in them. We selected most pathways SLCO5A1 participated on our site, such as , which may be useful for your reference. Also, other proteins which involved in the same pathway with SLCO5A1 were listed below. Creative BioMart supplied nearly all the proteins listed, you can search them on our site.
| Pathway Name | Pathway Related Protein |
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Protein Function
SLCO5A1 has several biochemical functions, for example, . Some of the functions are cooperated with other proteins, some of the functions could acted by SLCO5A1 itself. We selected most functions SLCO5A1 had, and list some proteins which have the same functions with SLCO5A1. You can find most of the proteins on our site.
| Function | Related Protein |
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Interacting Protein
SLCO5A1 has direct interactions with proteins and molecules. Those interactions were detected by several methods such as yeast two hybrid, co-IP, pull-down and so on. We selected proteins and molecules interacted with SLCO5A1 here. Most of them are supplied by our site. Hope this information will be useful for your research of SLCO5A1.
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References
- Isidor, B; Pichon, O; et al. Mesomelia-Synostoses Syndrome Results from Deletion of SULF1 and SLCO5A1 Genes at 8q13. AMERICAN JOURNAL OF HUMAN GENETICS 87:95-100(2010).
