2. Gene
  3. SLC9A2 - solute carrier family 9 member A2 Gene

SLC9A2 - solute carrier family 9 member A2 Gene

  • 基因
  • 蛋白
  • 疾病
  • 相关产品
  • 直系同源

中文名称：溶质载体家族 9 成员 A2

种属: Homo sapiens

同用名: NHE2

基因 ID: 6549 | 基因类型: protein coding

关于 SLC9A2

Cytogenetic location: 2q12.1 Genomic coordinates (GRCh38): 2:102,619,553-102,711,355 (from NCBI)

This gene has 3 transcripts (splice variants), 233 orthologues and 10 paralogues. Biased expression in stomach (RPKM 13.9), colon (RPKM 13.0) and 10 other tissues.

功能概要

该基因编码钠氢交换器 (NHE) 蛋白家族的一个成员。这些蛋白质通过将细胞内氢离子交换为外部钠离子参与钠离子转运，并有助于调节细胞 pH 值和体积。编码的蛋白质定位于顶膜并参与钠的顶端吸收。[RefSeq 提供，2016 年 6 月]

This gene encodes a member of the sodium-hydrogen exchanger (NHE) protein family. These proteins are involved in sodium-ion transport by exchanging intracellular hydrogen ions to external sodium ions and help in the regulation of cell pH and volume. The encoded protein is localized to the apical membrane and is involved in apical absorption of sodium. [provided by RefSeq, Jun 2016]

SLC9A2 基因产物(1)

mRNA Protein Name
NM_003048.6 NP_003039.2 sodium/hydrogen exchanger 2 precursor

SLC9A2 蛋白结构

Na_H_Exchanger

Na_H_Exchanger: Sodium/hydrogen exchanger family (84 - 484)

  • 0
  • 200
  • 400
  • 600
  • 812 a.a.
蛋白主名 其他名称

sodium/hydrogen exchanger 2

Na(+)/H(+) exchanger 2

关联疾病

疾病名称 别名
Diarrhea 1, Secretory Chloride, Congenital

DIAR1

Chloride Diarrhea, Congenital, Finnish Type

Congenital Secretory Chloride Diarrhea 1

Congenital Chloride Diarrhea Finnish Type

Congenital Chloride Diarrhea

Chloridorrhea, Congenital

Congenital Chloride Diarrhoea Finnish Type

Congenital Chloridorrhea

Congenital Secretory Chloride Diarrhoea 1

Chloridorrhea Congenital

Cld

Diarrhea 1 Secretory Chloride Congenital

Diarrhea, Type 1, Chloride, Secretory, Congenital
Short Bowel Syndrome

Short Gut Syndrome

Acquired Short Bowel Syndrome

Secondary Short Bowel Syndrome

Short Bowel Nos
Motility-Related Diarrhea
Spermatocele
Inflammatory Diarrhea
Osmotic Diarrhea
Secretory Diarrhea
Mucopolysaccharidosis, Type Ix

Mucopolysaccharidosis Type Ix

Hyaluronidase Deficiency

MPS9

Mps Ix

Mucopolysaccharidosis Ix

Mpsix

Mucopolysaccharidosis Type 9

Mucopolysaccharidosis 9
Diarrhea

Diarrhoea

Diarrhea Of Presumed Infectious Origin
疾病名称 别名
Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

相关产品

Pre-clinical Phase
生物活性分子 (2)
Cat. No. 产品名 作用方式
纯度 是否罕见病
HY-RS13342 SLC9A2 Human Pre-designed siRNA Set A Pre-designed Set / 否
HY-RS13350 SLC9B2 Human Pre-designed siRNA Set A Pre-designed Set / 否

直系同源

种属 基因名 来源 基因 ID
Felis catus SLC9A2 VGNC VGNC:65432
Canis familiaris SLC9A2 VGNC VGNC:46484
Rattus norvegicus SLC9A2 RGD RGD:3719
Mus musculus SLC9A2 MGD MGI:105075
Macaca mulatta SLC9A2 VGNC VGNC:77637
Bos taurus SLC9A2 VGNC VGNC:34939
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