| human | 遺伝子名 | SLC22A5 |
| 同義語(エイリアス) | OCTN2; FLJ46769; Solute carrier family 22 member 5; CDSP; Organic cation/carnitine transporter 2 | |
| SWISS-PROTのID | SWISS-PROT:O76082 | |
| EntrezGeneのID | EntrezGene:6584 | |
| その他のDBのID | HGNC:10969 |
| mouse | 遺伝子名 | Slc22a5 |
| 同義語(エイリアス) | Solute carrier family 22 member 5; jvs; Lstpl; Octn2; Organic cation/carnitine transporter 2 | |
| SWISS-PROTのID | SWISS-PROT:Q9Z0E8 | |
| EntrezGeneのID | EntrezGene:20520 | |
| その他のDBのID | MGI:1329012 |
| rat | 遺伝子名 | Slc22a5 |
| 同義語(エイリアス) | OCTN2; CT1; integral membrane transport protein; high-affinity carnitine transporter; Octn2; Organic cation/carnitine transporter 2; solute carrier family 22 member 5; UST2r; Solute carrier family 22 member 5; organic cation/carnitine transporter | |
| SWISS-PROTのID | SWISS-PROT:O70594 | |
| EntrezGeneのID | EntrezGene:29726 | |
| その他のDBのID | RGD:3702 |
本文中に表示されているデータベースの説明
出典:Wikipedia
出典:『Wikipedia』 (2010/06/17 01:42 UTC 版)
SLC22A5 is a membrane transport protein associated with primary carnitine deficiency.