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  2. RPL7A - ribosomal protein L7a Gene

RPL7A - ribosomal protein L7a Gene

中文名称:核糖体蛋白 L7a

种属: Homo sapiens

同用名: L7A; TRUP; SURF3

基因 ID: 6130 | 基因类型: protein coding

关于 RPL7A

Cytogenetic location: 9q34.2 Genomic coordinates (GRCh38): 9:133,348,218-133,351,426 (from NCBI)

This gene has 9 transcripts (splice variants), 1 gene allele, 137 orthologues and 3 paralogues. Ubiquitous expression in ovary (RPKM 1676.2), bone marrow (RPKM 795.5) and 25 other tissues.

功能概要

细胞质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 60S 亚基的一个组成部分。该蛋白属于核糖体蛋白 L7AE 家族。它可以与核激素受体的一个子类相互作用,包括甲状腺激素受体,并通过阻止它们与其 DNA 反应元件结合来抑制它们反式激活的能力。该基因包含在过剩基因簇中,这是一组非常紧密连锁的基因,它们不具有序列相似性。它与 U24、U36a、U36b 和 U36c 小核仁 RNA 基因共转录,这些基因分别位于其第二、第五、第四和第六个内含子中。该基因与 Trk 原癌基因重排形成嵌合癌基因 trk-2h,该基因编码一种癌蛋白,该癌蛋白由核糖体蛋白 L7a 的 N 末端组成,融合到 Trk 的受体酪氨酸激酶结构域。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]

Cytoplasmic ribosomes, 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 60S subunit. The protein belongs to the L7AE family of ribosomal proteins. It can interact with a subclass of nuclear hormone receptors, including Thyroid Hormone Receptor, and inhibit their ability to transactivate by preventing their binding to their DNA response elements. This gene is included in the surfeit gene cluster, a group of very tightly linked genes that do not share sequence similarity. It is co-transcribed with the U24, U36a, U36b, and U36c small nucleolar RNA genes, which are located in its second, fifth, fourth, and sixth introns, respectively. This gene rearranges with the Trk proto-oncogene to form the chimeric oncogene trk-2h, which encodes an oncoprotein consisting of the N terminus of ribosomal protein L7a fused to the receptor tyrosine kinase domain of Trk. 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]

RPL7A 基因产物(1)

mRNA Protein Name
NM_000972.3 NP_000963.1 60S ribosomal protein L7a
基因本体论
  • 分子功能
  • 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
15303970 GOA
enables structural constituent of ribosome IDA
IDA: 通过直接分析推断
23636399 GOA
细胞组分 GO 注释 逻辑证据 参考文献 来源
part of cytosolic large ribosomal subunit IDA
IDA: 通过直接分析推断
32669547 GOA
part of cytosolic large ribosomal subunit IPI
IPI: 通过物理相互作用推断
25901680 GOA
located in cytosolic ribosome IDA
IDA: 通过直接分析推断
23636399 GOA
located in membrane IDA
IDA: 通过直接分析推断
10848616 GOA
located in nucleolus IDA
IDA: 通过直接分析推断
25294810 GOA
located in ribosome IDA
IDA: 通过直接分析推断
10848616 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

RPL7A 蛋白结构

Ribosomal_L7Ae

Ribosomal_L7Ae: Ribosomal protein L7Ae/L30e/S12e/Gadd45 family (131 - 212)

  • 0
  • 100
  • 200
  • 266 a.a.
蛋白主名 其他名称

60S ribosomal protein L7a

PLA-X polypeptide

RPL7A 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
Intra RPL7A P62424 RPL7L1 Homo sapiens Q6DKI1
Anti Tag CoIP
33961781
Intra RPL7A P62424 RSL1D1 Homo sapiens O76021
Crosslink
30021884
Intra RPL7A P62424 RSL1D1 Homo sapiens O76021
Anti Tag CoIP
33961781
Intra RPL7A P62424 STAU1 Homo sapiens O95793
Anti Tag CoIP
33961781
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

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 RPL7A MGD MGI:1353472
Canis familiaris RPL7A VGNC VGNC:55813
Bos taurus RPL7A VGNC VGNC:49957
Rattus norvegicus RPL7A RGD RGD:1307586