1. Gene
  2. Slc22a5 - solute carrier family 22 member 5 Gene

Slc22a5 - solute carrier family 22 member 5 Gene

种属: Rattus norvegicus

同用名: CT1; OCTN2; UST2r

基因 ID: 29726 | 基因类型: protein coding

关于 Slc22a5

功能概要

Enables (R)-carnitine transmembrane transporter activity. Involved in (R)-carnitine transmembrane transport. Located in basolateral plasma membrane and cytosol. Human ortholog(s) of this gene implicated in Crohn's disease; cardiomyopathy; inherited metabolic disorder; and systemic primary carnitine deficiency disease. Orthologous to human SLC22A5 (solute carrier family 22 member 5). [provided by Alliance of Genome Resources, Apr 2022]

Slc22a5 基因产物(1)

mRNA Protein Name
NM_019269.1 NP_062142.1 solute carrier family 22 member 5
基因本体论
  • 分子功能
  • 生物过程
  • 细胞组分
生物过程 GO 注释 逻辑证据 参考文献 来源
involved in (R)-carnitine transmembrane transport IDA
IDA: 通过直接分析推断
10454528 RGD
involved in (R)-carnitine transmembrane transport IMP
IMP: 通过突变表型推断
28257821 RGD
involved in carnitine transport IDA
IDA: 通过直接分析推断
9792817 RGD
involved in carnitine transport IMP
IMP: 通过突变表型推断
16322553 RGD
involved in quaternary ammonium group transport IDA
IDA: 通过直接分析推断
10636865 RGD
involved in quaternary ammonium group transport IMP
IMP: 通过突变表型推断
10454528 RGD
细胞组分 GO 注释 逻辑证据 参考文献 来源
located in basolateral plasma membrane IDA
IDA: 通过直接分析推断
12080034 RGD
located in cytoplasm IDA
IDA: 通过直接分析推断
28257821 RGD
located in cytosol IDA
IDA: 通过直接分析推断
17995936 RGD
located in plasma membrane IDA
IDA: 通过直接分析推断
17995936 RGD
EXP:通过实验结果推断 IDA:通过直接分析推断 IPI:通过物理相互作用推断 IMP:通过突变表型推断 IGI:通过遗传相互作用推断 IEP:通过表达模式推断
蛋白主名 其他名称

solute carrier family 22 member 5

high-affinity carnitine transporter

high-affinity sodium-dependent carnitine cotransporter

integral membrane transport protein

organic cation/carnitine transporter 2

solute carrier family 22 (organic cation transporter), member 5

solute carrier famil

直系同源

种属 基因名 来源 基因 ID
Homo sapiens Slc22a5 NCBI NCBI:6584