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  2. RPS15A - ribosomal protein S15a Gene

RPS15A - ribosomal protein S15a Gene

中文名称:核糖体蛋白 S15a

种属: Homo sapiens

同用名: S15a; DBA20

基因 ID: 6210 | 基因类型: protein coding

关于 RPS15A

Cytogenetic location: 16p12.3 Genomic coordinates (GRCh38): 16:18,781,295-18,790,334 (from NCBI)

This gene has 13 transcripts (splice variants), 129 orthologues and is associated with 2 phenotypes. Ubiquitous expression in ovary (RPKM 1052.3), bone marrow (RPKM 811.7) and 25 other tissues.

功能概要

核糖体是催化蛋白质合成的细胞器,由一个小的 40S 亚基和一个大的 60S 亚基组成。这些亚基一起由 4 种 RNA 和大约 80 种结构不同的蛋白质组成。该基因编码的核糖体蛋白是 40S 亚基的一个组成部分。该蛋白属于核糖体蛋白 S8P 家族。它位于细胞质中。作为典型的编码核糖体蛋白的基因,该基因有多个经过处理的假基因分散在基因组中。[RefSeq 提供,2008 年 7 月]

Ribosomes, the organelles that catalyze protein synthesis, consist of a small 40S subunit and a large 60S subunit. Together these subunits are composed of 4 RNA species and approximately 80 structurally distinct proteins. This gene encodes a ribosomal protein that is a component of the 40S subunit. The protein belongs to the S8P family of ribosomal proteins. It is located in the cytoplasm. As is typical for genes encoding ribosomal proteins, there are multiple processed pseudogenes of this gene dispersed through the genome. [provided by RefSeq, Jul 2008]

RPS15A 基因产物(2)

mRNA Protein Name
NM_001019.5 NP_001010.2 40S ribosomal protein S15a
NM_001030009.2 NP_001025180.1 40S ribosomal protein S15a
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 protein binding IPI
IPI: 通过物理相互作用推断
24965446 GOA
enables structural constituent of ribosome IDA
IDA: 通过直接分析推断
23636399 GOA
生物过程 GO 注释 逻辑证据 参考文献 来源
involved in positive regulation of cell cycle IDA
IDA: 通过直接分析推断
15108328 GOA
involved in positive regulation of cell population proliferation IDA
IDA: 通过直接分析推断
15108328 GOA
involved in response to virus IDA
IDA: 通过直接分析推断
15108328 GOA
involved in ribosomal small subunit biogenesis IDA
IDA: 通过直接分析推断
34516797 GOA
细胞组分 GO 注释 逻辑证据 参考文献 来源
located in cytoplasm IDA
IDA: 通过直接分析推断
15108328 GOA
located in cytosolic ribosome IDA
IDA: 通过直接分析推断
23636399 GOA
part of cytosolic small ribosomal subunit IDA
IDA: 通过直接分析推断
8706699 GOA
part of small-subunit processome IDA
IDA: 通过直接分析推断
34516797 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

RPS15A 蛋白结构

Ribosomal_S8

Ribosomal_S8: Ribosomal protein S8 (6 - 129)

  • 0
  • 100
  • 130 a.a.
蛋白主名 其他名称

40S ribosomal protein S15a

small ribosomal subunit protein uS8

RPS15A 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
RPS15A P62244 KIF1B Homo sapiens O60333-2
Y2H Array
32814053
种属内
RPS15A P62244 KIF1B Homo sapiens O60333-2
Y2H Pooling
32814053
种属内
RPS15A P62244 KIF1B Homo sapiens O60333-2
Validated Y2H
32814053
种属内
RPS15A P62244 FGFR3 Homo sapiens P22607
Y2H Pooling
32814053
种属内
RPS15A P62244 FGFR3 Homo sapiens P22607
Validated Y2H
32814053
种属内
RPS15A P62244 FGFR3 Homo sapiens P22607
Y2H Array
32814053
种属内
RPS15A P62244 GSN Homo sapiens P06396
Y2H Pooling
32814053
种属内
RPS15A P62244 GSN Homo sapiens P06396
Validated Y2H
32814053
种属内
RPS15A P62244 GSN Homo sapiens P06396
Y2H Array
32814053
种属内
RPS15A P62244 HSPB1 Homo sapiens P04792
Validated Y2H
32814053
种属内
RPS15A P62244 HSPB1 Homo sapiens P04792
Y2H Array
32814053
种属内
RPS15A P62244 HSPB1 Homo sapiens P04792
Y2H Pooling
32814053
种属内
RPS15A P62244 RNF11 Homo sapiens Q9Y3C5
Y2H Array
32814053
种属内
RPS15A P62244 RNF11 Homo sapiens Q9Y3C5
Y2H Pooling
32814053
种属内
RPS15A P62244 RNF11 Homo sapiens Q9Y3C5
Validated Y2H
32814053
种属内
RPS15A P62244 PMP22 Homo sapiens A0A6Q8PF08
Y2H Pooling
32814053
种属内
RPS15A P62244 PMP22 Homo sapiens A0A6Q8PF08
Validated Y2H
32814053
种属内
RPS15A P62244 PMP22 Homo sapiens A0A6Q8PF08
Y2H Array
32814053
种属内
RPS15A P62244 WFS1 Homo sapiens O76024
Validated Y2H
32814053
种属内
RPS15A P62244 WFS1 Homo sapiens O76024
Y2H Pooling
32814053
种属内
RPS15A P62244 WFS1 Homo sapiens O76024
Y2H Array
32814053
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
Diamond-Blackfan Anemia 20

DBA20

Rps15a-Related Diamond-Blackfan Anemia

Diamond-Blackfan Anemia

Congenital Pure Red Cell Aplasia

Aase Syndrome

Erythrogenesis Imperfecta

Anemia, Diamond-Blackfan

Congenital Hypoplastic Anemia

Aase-Smith Ii Syndrome

Bds

Blackfan-Diamond Anemia

Congenital Prca

Congenital Hypoplastic Anemia, Blackfan-Diamond Type

Dba

Blackfan - Diamond Syndrome

Chronic Constitutional Pure Red Cell Anaemia

Anemia Diamond Blackfan Type

Anemia Congenital Erythroid Hypoplastic

Aregenerative Anemia Chronic Congenital

Blackfan Diamond Syndrome

Red Cell Aplasia, Pure Hereditary

Aase-Smith Syndrome Ii

Bda

Blackfan Diamond Anemia

Blackfan-Diamond Disease

Blackfan-Diamond Syndrome

Chronic Congenital Agenerative Anemia

Congenital Erythroid Hypoplastic Anemia

Congenital Hypoplastic Anemia Of Blackfan And Diamond

Congenital Pure Red Cell Anemia

Hypoplastic Congenital Anemia

Inherited Erythroblastopenia

Pure Hereditary Red Cell Aplasia

Anemia, Hypoplastic, Congenital

Anemia Hypoplastic Congenital

Fanconi Anemia

Constitutional Aplastic Anemia

Diamond-Blackfan Anemia 1

Aase Smith Syndrome 2

Congenital Red Cell Aplasia

Red Cell Aplasia Of Infants

Pure Red Cell Aplasia Of Infants

Congenital Red Cell Aplastic Anaemia

Congenital Pure Red Cell Anaemia

Congenital Erythroid Hypoplasia

Pearson Marrow-Pancreas Syndrome

Macrocytic Anemia

Anemia Macrocytic

Anemia, Macrocytic

Macrocytic Anaemia

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 RPS15A RGD RGD:619939
Mus musculus RPS15A MGD MGI:2389091