2. Gene
  3. Slc26a4 - solute carrier family 26 member 4 Gene

Slc26a4 - solute carrier family 26 member 4 Gene

  • 基因
  • 蛋白
  • 相关产品
  • 直系同源

种属: Rattus norvegicus

同用名: Pds

基因 ID: 29440 | 基因类型: protein coding

关于 Slc26a4

功能概要

Enables chloride transmembrane transporter activity and iodide transmembrane transporter activity. Involved in inorganic anion transport. Located in apical plasma membrane. Human ortholog(s) of this gene implicated in Pendred Syndrome; autosomal recessive nonsyndromic deafness 4; and goiter. Orthologous to human SLC26A4 (solute carrier family 26 member 4). [provided by Alliance of Genome Resources, Apr 2022]

Slc26a4 基因产物(1)

mRNA Protein Name
NM_019214.1 NP_062087.1 pendrin
基因本体论
  • 分子功能
  • 生物过程
  • 细胞组分
分子功能 GO 注释 逻辑证据 参考文献 来源
enables chloride transmembrane transporter activity IDA
IDA: 通过直接分析推断
12107249 RGD
enables chloride:bicarbonate antiporter activity IDA
IDA: 通过直接分析推断
11208611 RGD
enables iodide transmembrane transporter activity IDA
IDA: 通过直接分析推断
12107249 RGD
生物过程 GO 注释 逻辑证据 参考文献 来源
involved in inorganic anion transport IDA
IDA: 通过直接分析推断
12107249 RGD
细胞组分 GO 注释 逻辑证据 参考文献 来源
located in apical plasma membrane IDA
IDA: 通过直接分析推断
11208611 RGD
located in plasma membrane IDA
IDA: 通过直接分析推断
26791486 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

pendrin

Pendred syndrome homolog

sodium-independent chloride/iodide transporter

solute carrier family 26 (anion exchanger), member 4

相关产品

Pre-clinical Phase
生物活性分子 (5)
Cat. No. 产品名 作用方式
纯度 是否罕见病
HY-159706 S9-A13 Inhibitor 99.68% 否
HY-168735 SLC26A4-IN-1 Inhibitor 99.68% 否
HY-RS13138 SLC26A4 Human Pre-designed siRNA Set A Pre-designed Set / 否
HY-RS21256 Slc26a4 Mouse Pre-designed siRNA Set A Pre-designed Set / 否
HY-RS27775 Slc26a4 Rat Pre-designed siRNA Set A Pre-designed Set / 否

直系同源

种属 基因名 来源 基因 ID
Homo sapiens Slc26a4 NCBI NCBI:5172
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