SULT4A1 - sulfotransferase family 4A member 1 Gene

中文名称：磺基转移酶家族 4A 成员 1

种属: Homo sapiens

同用名: NST; BRSTL1; SULTX3; BR-STL-1; DJ388M5.3; hBR-STL-1

基因 ID: 25830 | 基因类型: protein coding

关于 SULT4A1

Cytogenetic location: 22q13.31 Genomic coordinates (GRCh38): 22:43,824,509-43,862,513 (from NCBI)

This gene has 4 transcripts (splice variants), 243 orthologues and 12 paralogues. Biased expression in brain (RPKM 30.9), duodenum (RPKM 4.1) 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。编码的蛋白质是一种脑特异性磺基转移酶，据信参与神经递质的代谢。该基因的多态性可能与精神分裂症的易感性有关。[RefSeq 提供，2008 年 7 月]

This gene encodes a member of the sulfotransferase family. The encoded protein is a brain-specific sulfotransferase believed to be involved in the metabolism of neurotransmitters. Polymorphisms in this gene may be associated with susceptibility to schizophrenia. [provided by RefSeq, Jul 2008]

SULT4A1 基因产物(1)

mRNA	Protein	Name
NM_014351.4	NP_055166.1	sulfotransferase 4A1

SULT4A1 蛋白结构

Sulfotransfer_1

0
100
200
284 a.a.

蛋白主名

其他名称

sulfotransferase 4A1

ST4A1

重组 SULT4A1 蛋白

目录号	产品名	蛋白编号	纯度
HY-P71344	SULT4A1 Protein, Human	Q9BR01 (M1-L284)	≥95%

关联疾病

疾病名称

别名

Anteroseptal Myocardial Infarction

Mixed Receptive-Expressive Language Disorder

Mitochondrial Dna Depletion Syndrome 1

MTDPS1	Mitochondrial Neurogastrointestinal Encephalopathy Syndrome, Tymp-Related
Myoneurogastrointestinal Encephalopathy Syndrome	Polip Syndrome
Mitochondrial Dna Depletion Syndrome, Type 1	Mngie, Tymp-Related
Polyneuropathy, Ophthalmoplegia, Leukoencephalopathy, And Intestinal Pseudoobstruction	Mitochondrial Dna Depletion Syndrome 1, Mngie Type
Mitochondrial Neurogastrointestinal Encephalomyopathy	Mitochondrial Neurogastrointestinal Encephalopathy Syndrome Tymp-Related
Myoneurogastrointestinal Encephalomyopathy	Polyneuropathy Ophthalmoplegia Leukoencephalopathy And Intestinal Pseudoobstruction
Mitochondrial Neurogastrointestinal Encephalopathy Syndrome

Neuronitis

Cercarial Dermatitis

Swimmer'S Itch	Cutaneous Schistosomiasis
Sea Bather'S Eruption	Clam-Digger'S Itch
Rice-Paddy Itch	Sea Bather'S Itch
Sawah Itch	Schistosomal Cercarial Dermatitis

N Syndrome

NSX	Intellectual Disability, Malformations, Chromosome Breakage, And Development Of T-Cell Leukemia

Schizophrenia

SCZD	Schizophrenia With Or Without An Affective Disorder
Schizophrenia 12	Schizophrenia, Susceptibility To
Schizophrenia-1	Dementia Praecox
Schizophrenia 1

Inferior Myocardial Infarction

Inferior Wall Myocardial Infarction

Schizotypal Personality Disorder

Schizotypal Personality

Phelan-Mcdermid Syndrome

Chromosome 22q13.3 Deletion Syndrome	22q13.3 Deletion Syndrome
Telomeric 22q13 Monosomy Syndrome	PHMDS
Deletion 22q13 Syndrome	22q13.3 Deletion
Deletion 22q13.3 Syndrome	Monosomy 22q13
Monosomy 22q13.3	22q13 Deletion Syndrome
Monosomy 22q13 Syndrome	22q13 Deletion
Chromosome Deletion

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

Cat. No.	产品名	作用方式	纯度	是否罕见病
HY-RS14022	SULT4A1 Human Pre-designed siRNA Set A	Pre-designed Sets	/	否

直系同源

种属	基因名	来源	基因 ID
Macaca mulatta	SULT4A1	VGNC	VGNC:78119
Rattus norvegicus	SULT4A1	RGD	RGD:69292
Canis familiaris	SULT4A1	VGNC	VGNC:46980
Mus musculus	SULT4A1	MGD	MGI:1888971
Felis catus	SULT4A1	VGNC	VGNC:65838
Bos taurus	SULT4A1	VGNC	VGNC:35469
Others	SULT4A1	NCBI

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