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  2. RELT - RELT TNF receptor Gene

RELT - RELT TNF receptor Gene

中文名称:RELT 肿瘤坏死因子受体

种属: Homo sapiens

同用名: AI3C; TRLT; TNFRSF19L

基因 ID: 84957 | 基因类型: protein coding

关于 RELT

Cytogenetic location: 11q13.4 Genomic coordinates (GRCh38): 11:73,376,399-73,397,474 (from NCBI)

This gene has 7 transcripts (splice variants), 197 orthologues, 21 paralogues and is associated with 2 phenotypes. Biased expression in bone marrow (RPKM 25.4), spleen (RPKM 6.1) and 8 other tissues.

功能概要

由该基因编码的蛋白质是 TNF 受体超家族的成员。这种受体在血液组织中特别丰富。它已被证明可以激活 NF-kappaB 通路并选择性地结合 TNF 受体相关因子 1 (TRAF1) 。该受体能够在 CD3 信号传导存在的情况下刺激 T 细胞增殖,这表明其在免疫反应中的调节作用。已经报道了编码相同蛋白质的该基因的两个选择性剪接的转录物变体。[RefSeq 提供,2008 年 7 月]

The protein encoded by this gene is a member of the TNF-receptor superfamily. This receptor is especially abundant in hematologic tissues. It has been shown to activate the NF-kappaB pathway and selectively bind TNF receptor-associated factor 1 (TRAF1). This receptor is capable of stimulating T-cell proliferation in the presence of CD3 signaling, which suggests its regulatory role in immune response. Two alternatively spliced transcript variants of this gene encoding the same protein have been reported. [provided by RefSeq, Jul 2008]

RELT 基因产物(2)

mRNA Protein Name
NM_032871.4 NP_116260.2 tumor necrosis factor receptor superfamily member 19L precursor
NM_152222.2 NP_689408.1 tumor necrosis factor receptor superfamily member 19L 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
16530727 GOA
生物过程 GO 注释 逻辑证据 参考文献 来源
involved in amelogenesis IMP
IMP: 通过突变表型推断
30506946 GOA
involved in apoptotic process IMP
IMP: 通过突变表型推断
16530727 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

RELT 蛋白结构

RELT

RELT: Tumour necrosis factor receptor superfamily member 19 (163 - 204)

  • 0
  • 100
  • 200
  • 300
  • 400
  • 430 a.a.
蛋白主名 其他名称

tumor necrosis factor receptor superfamily member 19L

RELT tumor necrosis factor receptor

重组 RELT 蛋白

目录号 产品名 蛋白编号 纯度
HY-P71258 RELT Protein, Human (HEK293, Fc) Q969Z4 (S26-A160) ≥95%

关联疾病

疾病名称 别名
Amelogenesis Imperfecta, Type Iiic

AI3C

Amelogenesis Imperfecta, Hypocalcification Type, Autosomal Recessive

Amelogenesis Imperfecta Type 3c

Amelogenesis Imperfecta, Type 3c

Amelogenesis Imperfecta Type Iiic

Autosomal Recessive Amelogenesis Imperfecta Hypocalcification Type

Amelogenesis Imperfecta 3c

Hypoplastic Amelogenesis Imperfecta

Amelogenesis Imperfecta Type 1

Amelogenesis Imperfecta, Hypoplastic Type

Amelogenesis Imperfecta Local Hypoplastic Form

Amelogenesis Imperfecta

Ai

Congenital Enamel Hypoplasia

Al - [Amelogenesis Imperfecta]

Myopathy, Congenital, Compton-North

Compton-North Congenital Myopathy

MYPCN

Congenital Lethal Myopathy, Compton-North Type

Amelogenesis Imperfecta, Hypomaturation Type, Iia5

Amelogenesis Imperfecta Hypomaturation Type 2a5

AI2A5

Amelogenesis Imperfecta, Type Iia5

Amelogenesis Imperfecta Hypomaturation Type Iia5

Amelogenesis Imperfecta Type Iia5

Amelogenesis Imperfecta, Hypomaturation Type, 2a5

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
Felis catus RELT VGNC VGNC:64568
Rattus norvegicus RELT RGD RGD:1305381
Bos taurus RELT VGNC VGNC:33862
Canis familiaris RELT VGNC VGNC:45471
Mus musculus RELT MGD MGI:2443373
Macaca mulatta RELT VGNC VGNC:76728
Others RELT NCBI