1. Gene
  2. RPL22L1 - ribosomal protein L22 like 1 Gene

RPL22L1 - ribosomal protein L22 like 1 Gene

中文名称:核糖体蛋白 L22 样 1

种属: Homo sapiens

基因 ID: 200916 | 基因类型: protein coding

关于 RPL22L1

This gene has 6 transcripts (splice variants), 270 orthologues and 1 paralogue. Ubiquitous expression in bone marrow (RPKM 15.2), appendix (RPKM 13.6) and 25 other tissues.

功能概要

预测启用 RNA 结合活性。预计是核糖体的结构成分。预计参与细胞质翻译。预测位于核糖体中。 [由基因组资源联盟提供,2022 年 4 月]

Predicted to enable RNA binding activity. Predicted to be a structural constituent of ribosome. Predicted to be involved in cytoplasmic translation. Predicted to be located in ribosome. [provided by Alliance of Genome Resources, Apr 2022]

RPL22L1 基因产物(2)

mRNA Protein Name
NM_001099645.2 NP_001093115.1 60S ribosomal protein L22-like 1 isoform 1
NM_001320451.2 NP_001307380.1 60S ribosomal protein L22-like 1 isoform 2
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 protein binding IPI
IPI: 通过物理相互作用推断
32296183 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

RPL22L1 蛋白结构

Ribosomal_L22e

Ribosomal_L22e: Ribosomal L22e protein family (10 - 119)

  • 0
  • 100
  • 122 a.a.
蛋白主名 其他名称

60S ribosomal protein L22-like 1

large ribosomal subunit protein eL22-like 1

RPL22L1 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
RPL22L1 Q6P5R6 SDCBP2 Homo sapiens Q9H190 32296183
种属内
RPL22L1 Q6P5R6 SDCBP2 Homo sapiens Q9H190 32296183
种属内
RPL22L1 Q6P5R6 SDCBP2 Homo sapiens Q9H190 32296183
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
Colon Sarcoma

Colonic Sarcoma

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

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 RPL22L1 MGD MGI:1915278
Rattus norvegicus RPL22L1 RGD RGD:1309517
Canis familiaris RPL22L1 VGNC VGNC:45716
Felis catus RPL22L1 VGNC VGNC:102832
Macaca mulatta RPL22L1 VGNC VGNC:84091
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