1. Gene
  2. SHB - SH2 domain containing adaptor protein B Gene

SHB - SH2 domain containing adaptor protein B Gene

中文名称:含 SH2 结构域的衔接蛋白 B

种属: Homo sapiens

同用名: bA3J10.2

基因 ID: 6461 | 基因类型: protein coding

关于 SHB

Cytogenetic location: 9p13.1 Genomic coordinates (GRCh38): 9:37,915,898-38,069,227 (from NCBI)

This gene has 1 transcript (splice variant), 122 orthologues and 3 paralogues. Ubiquitous expression in liver (RPKM 4.9), kidney (RPKM 3.8) and 25 other tissues.

功能概要

启用磷酸酪氨酸残基结合活性。预计参与多个过程,包括血管生成;凋亡过程;和信号转导。预计在几个过程的上游或内部起作用,包括造血干细胞增殖;卵母细胞成熟的负调节;和免疫反应的正调节。位于细胞质核糖核蛋白颗粒;胞质溶胶;和核质。 [由基因组资源联盟提供,2022 年 4 月]

Enables phosphotyrosine residue binding activity. Predicted to be involved in several processes, including angiogenesis; apoptotic process; and signal transduction. Predicted to act upstream of or within several processes, including hematopoietic stem cell proliferation; negative regulation of oocyte maturation; and positive regulation of immune response. Located in cytoplasmic ribonucleoprotein granule; cytosol; and nucleoplasm. [provided by Alliance of Genome Resources, Apr 2022]

SHB 基因产物(1)

mRNA Protein Name
NM_003028.3 NP_003019.2 SH2 domain-containing adapter protein B
基因本体论
  • 分子功能
分子功能 GO 注释 逻辑证据 参考文献 来源
enables phosphotyrosine residue binding IPI
IPI: 通过物理相互作用推断
20624904 GOA
enables protein binding IPI
IPI: 通过物理相互作用推断
17112510 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

SHB 蛋白结构

SH2

SH2: SH2 domain (410 - 485)

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

SH2 domain-containing adapter protein B

SHB (Src homology 2 domain containing) adaptor protein B

SHB 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
SHB Q15464 MET Homo sapiens P08581
FPS
24728074
种属内
SHB Q15464 KIT Homo sapiens P10721
FPS
24728074
种属内
SHB Q15464 ABL1 Homo sapiens P00519 17112510
种属内
SHB Q15464 ABL1 Homo sapiens P00519 17112510
种属间: 跨种属相互作用 种属内: 同种属相互作用

关联疾病

疾病名称 别名
Sulfhemoglobinemia
Horner'S Syndrome

Horner Syndrome

Bernard-Horner Syndrome

Oculosympathetic Palsy

Bernard Horner Syndrome

Cervical Sympathetic Paralysis

Von Passow Syndrome

Cervical Sympathetic Dystrophy

Methemoglobinemia
Familial Isolated Hypoparathyroidism

Fih

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
Canis familiaris SHB VGNC VGNC:46138
Bos taurus SHB VGNC VGNC:34588
Rattus norvegicus SHB RGD RGD:1565350
Mus musculus SHB MGD MGI:98294
Macaca mulatta SHB VGNC VGNC:82236
Macaca fascicularis SHB NCBI NCBI:102135347
Others SHB NCBI