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  2. SULT2A1 - sulfotransferase family 2A member 1 Gene

SULT2A1 - sulfotransferase family 2A member 1 Gene

中文名称:磺基转移酶家族 2A 成员 1

种属: Homo sapiens

同用名: HST; ST2; STD; hSTa; DHEAS; ST2A1; ST2A3; DHEA-ST; SULT2A3; DHEA-ST8

基因 ID: 6822 | 基因类型: protein coding

关于 SULT2A1

Cytogenetic location: 19q13.33 Genomic coordinates (GRCh38): 19:47,870,467-47,886,315 (from NCBI)

This gene has 1 transcript (splice variant), 781 orthologues and 12 paralogues. Biased expression in liver (RPKM 300.0), adrenal (RPKM 86.0) and 2 other tissues.

功能概要

该基因编码磺基转移酶家族的一个成员。磺基转移酶通过将这些物质转化为更亲水的水溶性硫酸盐结合物,从而帮助药物和内源性化合物的代谢,这些结合物可以很容易地排出体外。这种蛋白质催化肝脏和肾上腺中类固醇和胆汁酸的硫酸化,并且可能在患有多囊卵巢综合征的女性的遗传性肾上腺雄激素过多中起作用。[RefSeq 提供,2010 年 3 月]

This gene encodes a member of the sulfotransferase family. Sulfotransferases aid in the metabolism of drugs and endogenous compounds by converting these substances into more hydrophilic water-soluble sulfate conjugates that can be easily excreted. This protein catalyzes the sulfation of Steroids and bile acids in the liver and adrenal glands, and may have a role in the inherited adrenal androgen excess in women with polycystic ovary syndrome. [provided by RefSeq, Mar 2010]

SULT2A1 基因产物(1)

mRNA Protein Name
NM_003167.4 NP_003158.2 sulfotransferase 2A1
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 3'-phosphoadenosine 5'-phosphosulfate binding IDA
IDA: 通过直接分析推断
10854859 GOA
enables alcohol sulfotransferase activity IDA
IDA: 通过直接分析推断
7854148 GOA
enables bile-salt sulfotransferase activity IDA
IDA: 通过直接分析推断
1588921 GOA
enables protein binding IPI
IPI: 通过物理相互作用推断
21988832 GOA
enables steroid sulfotransferase activity IDA
IDA: 通过直接分析推断
23207770 GOA
enables steroid sulfotransferase activity IMP
IMP: 通过突变表型推断
29671343 GOA
enables sulfotransferase activity IDA
IDA: 通过直接分析推断
19548878 GOA
生物过程 GO 注释 逻辑证据 参考文献 来源
involved in 3'-phosphoadenosine 5'-phosphosulfate metabolic process IDA
IDA: 通过直接分析推断
23207770 GOA
involved in cholesterol metabolic process IDA
IDA: 通过直接分析推断
19589875 GOA
involved in ethanol catabolic process IDA
IDA: 通过直接分析推断
23207770 GOA
involved in steroid metabolic process IDA
IDA: 通过直接分析推断
1588921 GOA
involved in steroid metabolic process IMP
IMP: 通过突变表型推断
29671343 GOA
acts upstream of or within sulfation IDA
IDA: 通过直接分析推断
19548878 GOA
involved in sulfation IDA
IDA: 通过直接分析推断
20056724 GOA
involved in thyroid hormone metabolic process IDA
IDA: 通过直接分析推断
10199779 GOA
involved in xenobiotic metabolic process IDA
IDA: 通过直接分析推断
7854148 GOA
细胞组分 GO 注释 逻辑证据 参考文献 来源
located in cytosol IDA
IDA: 通过直接分析推断
2268288 GOA
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

SULT2A1 蛋白结构

Sulfotransfer_1

Sulfotransfer_1: Sulfotransferase domain (34 - 277)

  • 0
  • 100
  • 200
  • 285 a.a.
蛋白主名 其他名称

sulfotransferase 2A1

alcohol/hydroxysteroid sulfotransferase

SULT2A1 蛋白互作信息

分类
蛋白名称 蛋白编号 互作蛋白 互作蛋白种属 互作蛋白编号 实验方法 参考文献
种属内
SULT2A1 Q06520 SULT1B1 Homo sapiens O43704
Y2H Prey Pooling
32296183
种属内
SULT2A1 Q06520 SULT1B1 Homo sapiens O43704
Y2H Array
32296183
种属内
SULT2A1 Q06520 STAT3 Homo sapiens P40763
Y2H
21988832
种属内
SULT2A1 Q06520 NIF3L1 Homo sapiens Q9GZT8
Validated Y2H
32296183
种属内
SULT2A1 Q06520 NIF3L1 Homo sapiens Q9GZT8
Y2H Array
32296183
种属内
SULT2A1 Q06520 NIF3L1 Homo sapiens Q9GZT8
Y2H Prey Pooling
32296183
种属间: 跨种属相互作用 种属内: 同种属相互作用

重组 SULT2A1 蛋白

目录号 产品名 蛋白编号 纯度
HY-P71343 SULT2A1 Protein, Human (His) Q06520 (S2-E285) ≥95%

SULT2A1 抗体

目录号 产品名 应用 反应物种
HY-P82116 Sulfotransferase 2A1 Antibody (YA1861) WB, IHC-P, ICC/IF, FC Human, Mouse, Rat

关联疾病

疾病名称 别名
Mixed Epithelial Stromal Tumour
Adrenal Cortical Adenoma

Adrenocortical Adenoma

Adenoma Adrenocortical

Polycystic Ovary Syndrome

Polycystic Ovarian Syndrome

Pcos

Polycystic Ovarian Disease

Polycystic Ovaries

Stein-Leventhal Syndrome

Multicystic Ovaries

Polycystic Ovary

Sclerocystic Ovaries

Sclerocystic Ovary Syndrome

Stein-Leventhal Synd.

Cystic Disease Of Ovaries

Cystic Disease Of Ovary

Pco

Pcod

Sclerocystic Ovarian Degeneration

Polycystic Ovary Syndrome, Susceptibility To

Pcos - [Polycystic Ovary Syndrome]

Polycystic Ovary Nos

Pco - [Polycystic Ovary]

Conn'S Syndrome

Cushing Syndrome

Hyperaldosteronism

Primary Hyperaldosteronism

Hypercortisolism

Primary Aldosteronism

Cushing'S Syndrome

Adrenal Gland Hyperfunction

Conn Syndrome

Hyperadrenalism

Ectopic Acth Syndrome

Hyperadrenocorticism

Cushing Disease

Cushing'S Disease

Adrenal Cortex Adenoma

Corticotroph Pituitary Adenoma

Pituitary Corticotroph Micro-Adenoma

Pituitary-Dependent Cushing Syndrome

Pituitary Acth Hypersecretion

Acth Syndrome, Ectopic

Acth-Secreting Pituitary Adenoma

Adrenal Hyperfunction Resulting From Pituitary Acth Excess

Ectopic Adrenocorticotropic Hormone Syndrome

Nodular Primary Adrenocortical Dysplasia

Pituitary Dependent Cushing Syndrome

Pituitary Cushing Syndrome

Pituitary-Dependant Cushing Syndrome

Pituitary-Dependant Hypercortisolism

Pituitary-Dependant Hypercortisolism Disorder

Aldosteronism Primary

Acth Syndrome Ectopic

Adrenal Cushing'S Syndrome

Adrenal Cortical Adenoma

Cushing Syndrome Nos

Cortisol Hypersecretion

Corticoadrenal Hypersecretion

Cushing Syndrome Secondary To Ectopic Acth-Secretion

Ectopic Cushing Syndrome

Hypercortisolism Due To Nonpituitary Tumour

Ectopic Acth - [Adrenocorticotropic Hormone] Secretion

Ectopic Acth - [Adrenocorticotropic Hormone] Secretion Causing Cushing Syndrome

Idiopathic Aldosteronism

Aldosteronism

Primary Aldosteronism Due To Bilateral Adrenal Hyperplasia

Primary Aldosteronism Due To Adrenal Hyperplasia

Cholangitis, Primary Sclerosing

Primary Sclerosing Cholangitis

PSC

Sclerosing Cholangitis

Cholangitis, Sclerosing

Cholangitis Primary Sclerosing

Psc - [Primary Sclerosing Cholangitis]

Cortisone Reductase Deficiency

11-Alpha Beta-Hydroxysteroid Dehydrogenase Type I Deficiency Of

Cortrd

Hsd 11b1 Deficiency

Asperger Syndrome

Asperger Disorder

Asperger Syndrome, Susceptibility To

Adrenal Cortical Carcinoma

Adrenocortical Carcinoma

Adrenal Cortex Carcinoma

Carcinoma Of The Adrenal Cortex

Acc

Adrenocortical Cancer

Carcinoma Adrenocortical

Adult Hepatocellular Carcinoma

Adult Primary Hepatocellular Carcinoma

Adult Hepatoma

Adult Hcc

Lipoid Congenital Adrenal Hyperplasia

Congenital Adrenal Hyperplasia

Congenital Lipoid Adrenal Hyperplasia Due To Star Deficency

Congenital Lipoid Adrenal Hyperplasia

Lipoid Cah

Lipoid Adrenal Hyperplasia

Adrenal Hyperplasia 1

Cah

Clah

LCAH

Adrenal Hyperplasia I

Lipoid Hyperplasia, Congenital, Of Adrenal Cortex With Male Pseudohermaphroditism

Congenital Adrenal Hyperplasia Lipoid

Adrenal Hyperplasia, Congenital

Congenital Adrenal Hyperplasia, Lipoid

AH1

Congenital Lipoid Hyperplasia Of Adrenal Cortex With Male Pseudohermaphroditism

Adrenal Hyperplasia Congenital

Hyperplasia, Adrenal, Lipoid, Congenital

Congenital Adrenogenital Disorders Associated With Enzyme Deficiency

Congenital Adrenal Cortical Hyperplasia

Congenital Adrenal Gland Hyperplasia

Congenital Adrenogenital Syndrome

Congenital Hyperadrenocorticism

Congenital Adrenogenitalism

Congenital Female Adrenal Pseudohermaphroditism

Intrahepatic Cholestasis Of Pregnancy

Recurrent Intrahepatic Cholestasis Of Pregnancy

Gravidic Intrahepatic Cholestasis

Pregnancy-Related Cholestasis

Icp

Pregnancy Related Cholestasis

Cholestasis, Intrahepatic Of Pregnancy

Familial Intrahepatic Cholestasis Of Pregnancy

Familial Recurrent Intrahepatic Cholestasis Of Pregnancy

Ricp

Obstetric Cholestasis

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

直系同源

种属 基因名 来源 基因 ID
Rattus norvegicus SULT2A1 RGD RGD:621337
Macaca mulatta SULT2A1 VGNC VGNC:78053
Others SULT2A1 NCBI