1. Gene
  2. TNFRSF18 - TNF receptor superfamily member 18 Gene

TNFRSF18 - TNF receptor superfamily member 18 Gene

中文名称:TNF 受体超家族成员 18

种属: Homo sapiens

同用名: AITR; GITR; CD357; GITR-D; ENERGEN

基因 ID: 8784 | 基因类型: protein coding

关于 TNFRSF18

Cytogenetic location: 1p36.33 Genomic coordinates (GRCh38): 1:1,203,508-1,206,592 (from NCBI)

This gene has 4 transcripts (splice variants), 562 orthologues and 21 paralogues. Biased expression in skin (RPKM 4.0), appendix (RPKM 1.0) and 12 other tissues.

功能概要

该基因编码 TNF 受体超家族的一个成员。编码的受体已被证明在 T 细胞激活后表达增加,并且它被认为在 CD25 (+) CD4 (+) 调节性 T 细胞维持的显性免疫自身耐受中发挥关键作用。小鼠基因敲除研究也表明该受体在调节 CD3 驱动的 T 细胞激活和程序性细胞死亡中的作用。已经报道了编码不同同种型的该基因的三种可变剪接转录物变体。[RefSeq 提供,2011 年 2 月]

This gene encodes a member of the TNF-receptor superfamily. The encoded receptor has been shown to have increased expression upon T-cell activation, and it is thought to play a key role in dominant immunological self-tolerance maintained by CD25(+)CD4(+) regulatory T cells. Knockout studies in mice also suggest the role of this receptor is in the regulation of CD3-driven T-cell activation and programmed cell death. Three alternatively spliced transcript variants of this gene encoding distinct isoforms have been reported. [provided by RefSeq, Feb 2011]

TNFRSF18 基因产物(3)

mRNA Protein Name
NM_004195.3 NP_004186.1 tumor necrosis factor receptor superfamily member 18 isoform 1 precursor
NM_148901.2 NP_683699.1 tumor necrosis factor receptor superfamily member 18 isoform 2 precursor
NM_148902.2 NP_683700.1 tumor necrosis factor receptor superfamily member 18 isoform 3 precursor
基因本体论
  • 分子功能
  • 生物过程
分子功能 GO 注释 逻辑证据 参考文献 来源
enables protein binding IPI
IPI: 通过物理相互作用推断
18040044 GOA
生物过程 GO 注释 逻辑证据 参考文献 来源
involved in positive regulation of cell adhesion IMP
IMP: 通过突变表型推断
23892569 GOA
involved in positive regulation of leukocyte migration IMP
IMP: 通过突变表型推断
23892569 GOA
involved in positive regulation of tyrosine phosphorylation of STAT protein IMP
IMP: 通过突变表型推断
23892569 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
蛋白主名 其他名称

tumor necrosis factor receptor superfamily member 18

TNF receptor superfamily activation-inducible protein

TNFRSF18 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
TNFRSF18 Q9Y5U5 TNFSF18 Homo sapiens Q9UNG2
SPR
18378892
种属间: 跨种属相互作用 种属内: 同种属相互作用

重组 TNFRSF18 蛋白

目录号 产品名 蛋白编号 纯度
HY-P70683 GITR Protein, Human (HEK293, hFc) Q9Y5U5 (Q26-E161) ≥95%
HY-P70822 GITR Protein, Human (T45A, HEK293, mFc) Q9Y5U5 (Q26-E161, T45A) ≥95%
HY-P73076 GITR Protein, Human (HEK293, His) Q9Y5U5 (Q26-E161) ≥95%
HY-P75166 GITR Protein, Human (Biotinylated, HEK293, Fc-Avi) Q9Y5U5 (Q26-E161) ≥95%
HY-P78137 GITR Protein, Human (Biotinylated, HEK293, His-Avi) Q9Y5U5 (Q26-E161) ≥95%

关联疾病

疾病名称 别名
Immunodysregulation, Polyendocrinopathy, And Enteropathy, X-Linked

IPEX

X-Linked Autoimmunity-Allergic Dysregulation Syndrome

Xlaad

Diarrhea, Polyendocrinopathy, Fatal Infection Syndrome, X-Linked

Ipex Syndrome

Insulin-Dependent Diabetes Mellitus Secretory Diarrhea Syndrome

Iddm-Secretory Diarrhea Syndrome

Dmsd

Autoimmunity-Immunodeficiency Syndrome, X-Linked

Enteropathy, Autoimmune, With Hemolytic Anemia And Polyendocrinopathy

Xpid

Diabetes Mellitus, Congenital Insulin-Dependent, With Fatal Secretory Diarrhea

Immune Dysregulation-Polyendocrinopathy-Enteropathy-X-Linked Syndrome

Polyendocrinopathy, Immune Dysfunction, And Diarrhea, X-Linked

Autoimmune Enteropathy Type 1

Immunodeficiency, Polyendocrinopathy, And Enteropathy, X-Linked

Immunodeficiency, Polyendocrinopathy, And Enteropathy, X-Linked, Formerly

Immunodeficiency, Polyendocrinopathy, Enteropathy X-Linked Syndrome

Immunodysregulation, Polyendocrinopathy And Enteropathy X-Linked

Autoimmunity-Immunodeficiency Syndrome X-Linked

Iddm Secretory Diarrhea Syndrome

Polyendocrinopathy, Immune Dysfunction And Diarrhea X-Linked

Immune Dysregulation, Polyendocrinopathy, Enteropathy, X-Linked Syndrome

Immunodeficiency Polyendocrinopathy, Enteropathy, X-Linked Syndrome

X-Linked Autoimmunity-Immunodeficiency Syndrome

Immunodeficiency, Polyendocrinopathy, And Enteropathy X-Linked Syndrome

X-Linked Syndrome Of Polyendocrinopathy, Immune Dysfunction, And Diarrhea

Diverticulitis
Immunodeficiency 41 With Lymphoproliferation And Autoimmunity

Cd25 Deficiency

Immunodeficiency Due To Cd25 Deficiency

IMD41

Interleukin 2 Receptor, Alpha, Deficiency Of

Il2ra Deficiency

Immunodeficiency 41

Interleukin-2 Receptor Alpha Chain Deficiency

Interleukin 2 Receptor Alpha Deficiency

Interleukin-2 Receptor, Alpha Chain, Deficiency Of

Immunodeficiency, Type 41 With Lymphoproliferation And Autoimmunity

Autoimmune Disease

Autoimmune Diseases

Autoimmune Hypersensitivity Disease

Hypersensitivity Reaction Type Ii Disease

Type Ii Hypersensitivity Reaction Disease

Common Variable Immunodeficiency

Cvid

Common Variable Agammaglobulinemia

Common Variable Immune Deficiency

Acquired Hypogammaglobulinemia

Hypogamma-Globulinemia, Acquired

Idiopathic Immunoglobulin Deficiency

Primary Antibody Deficiency

Primary Hypogammaglobulinemia

Acquired Agammaglobulinemia

Sporadic Hypogammaglobulinemia

Common Variable Hypogamma-Globulinemia

Immunoglobulin Deficiency, Late-Onset

Common Variable Hypogammaglobulinemia

Immunodeficiency, Common Variable

Dermatitis, Atopic, 7

ATOD7

Dermatitis, Atopic, Susceptibility To, 7

Atopic Dermatitis 7

Dermatitis, Atopic 7

Rheumatoid Arthritis

RA

Arthritis, Rheumatoid

Rheumatoid Arthritis, Susceptibility To

Arthritis Or Polyarthritis, Rheumatic

Atrophic Arthritis

Rheumatism Arthritis

Rheumatoid Polyarthritis

Parotid Gland Adenoid Cystic Carcinoma

Adenoid Cystic Carcinoma Of Parotid Gland

Immune Deficiency Disease

Immunodeficiency

Primary Immunodeficiency

Primary Immunodeficiency Disease

Immunologic Deficiency Syndromes

Hypoimmunity

Immune Deficiency Disorder

Immunodeficiency Syndrome

Immune Disorder

Primary Immune Deficiency Disorder

Immune System Diseases

Human Immunodeficiency Virus Infection

Hiv - [Human Immunodeficiency Virus Infection]

Hiv Positive Nos

Hiv Disease

Acquired Immune Deficiency Syndrome-Related Complex

Aids-Like Syndrome

Aids-Related Complex Nos

Arc - [Aids-Related Complex]

Immunodeficiency Due To Human Immunodeficiency Virus Infection

Unspecified Human Immunodeficiency Virus Disease

Hiv Disease Nos

Human Immunodeficiency Virus Positive Nos

Hiv Nos

Deficiency Of Complement Initial Pathway

Deficiency Of Complement Terminal Pathway

Cfdd - [Complement Factor D Deficiency]

Immunodeficiency With Nk-Cell - [Natural-Killer Cell] Deficiency

Nonfamilial Hypogammaglobulinaemia

Common Variable Immune Deficiency

Nonfamilial Agammaglobulinaemia

Common Variable Agammaglobulinaemia

Agammaglobulinaemia Nos

Agammaglobulinaemia Antibody Deficiency Syndrome

Hypogammaglobulinaemia Antibody Deficiency Syndrome

Acquired Agammaglobulinaemia Nos

Hypogammaglobulinaemia Nos

Hyper Igm

Dermatitis, Atopic

Atopic Dermatitis

Atopic Eczema

Dermatitis, Atopic, Susceptibility To, 1

Atod

Eczema, Atopic

Dermatitis, Atopic 1

Allergic Dermatitis

Atopic Neurodermatitis

Besnier'S Prurigo

Dermatitis, Atopic, 1

Dermatitis Atopic

Eczema

Besnier Prurigo

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
Mus musculus TNFRSF18 MGD MGI:894675
Macaca mulatta TNFRSF18 VGNC VGNC:78587
Rattus norvegicus TNFRSF18 RGD RGD:1565872
Canis familiaris TNFRSF18 VGNC VGNC:47660
Felis catus TNFRSF18 VGNC VGNC:66406
Bos taurus TNFRSF18 VGNC VGNC:36163
Macaca fascicularis TNFRSF18 NCBI NCBI:102146362
Others TNFRSF18 NCBI