1. Gene
  2. RSL24D1 - ribosomal L24 domain containing 1 Gene

RSL24D1 - ribosomal L24 domain containing 1 Gene

中文名称:含核糖体 L24 域 1

种属: Homo sapiens

同用名: L30; RLP24; RPL24; TVAS3; RPL24L; C15orf15; HRP-L30-iso

基因 ID: 51187 | 基因类型: protein coding

关于 RSL24D1

Cytogenetic location: 15q21.3 Genomic coordinates (GRCh38): 15:55,180,806-55,196,941 (from NCBI)

This gene has 12 transcripts (splice variants), 206 orthologues and 1 paralogue. Ubiquitous expression in bone marrow (RPKM 88.8), ovary (RPKM 69.7) and 25 other tissues.

功能概要

该基因编码的蛋白质与人类核糖体蛋白 L24 具有低水平的序列相似性。尽管该基因在序列数据库中被称为 RPL24、L30 和 60S 核糖体蛋白 L30 同源基因,但它不同于正式命名为 RPL24 (其本身被称为核糖体蛋白 L30) 和 RPL30 的人类基因。由该基因编码的蛋白质定位于核仁,被认为在 60S 核糖体亚基的生物合成中发挥作用。该基因的确切功能目前尚不清楚。该基因利用替代性聚腺苷酸化信号并具有多个假基因。[RefSeq 提供,2012 年 7 月]

This gene encodes a protein sharing a low level of sequence similarity with human ribosomal protein L24. Although this gene has been referred to as RPL24, L30, and 60S ribosomal protein L30 isolog in the sequence databases, it is distinct from the human genes officially named RPL24 (which itself has been referred to as ribosomal protein L30) and RPL30. The protein encoded by this gene localizes to the nucleolus and is thought to play a role in the biogenesis of the 60S ribosomal subunit. The precise function of this gene is currently unknown. This gene utilizes alternative polyadenylation signals and has multiple pseudogenes. [provided by RefSeq, Jul 2012]

RSL24D1 基因产物(1)

mRNA Protein Name
NM_016304.3 NP_057388.1 probable ribosome biogenesis protein RLP24
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
16189514 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

RSL24D1 蛋白结构

Ribosomal_L24e

Ribosomal_L24e: Ribosomal protein L24e (1 - 64)

  • 0
  • 100
  • 163 a.a.
蛋白主名 其他名称

probable ribosome biogenesis protein RLP24

60S ribosomal protein L30 isolog

RSL24D1 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 RSL24D1 Q9UHA3 FAM9B Homo sapiens Q8IZU0
Y2H Prey Pooling
25416956
Intra RSL24D1 Q9UHA3 FAM9B Homo sapiens Q8IZU0
Y2H Array
25416956
Intra RSL24D1 Q9UHA3 CDC23 Homo sapiens Q9UJX2
Validated Y2H
25416956
Intra RSL24D1 Q9UHA3 DNMT3L Homo sapiens Q9UJW3
Y2H Array
32296183
Intra RSL24D1 Q9UHA3 DNMT3L Homo sapiens Q9UJW3
Validated Y2H
32296183
Intra RSL24D1 Q9UHA3 DNMT3L Homo sapiens Q9UJW3
Y2H Prey Pooling
25416956
Intra RSL24D1 Q9UHA3 DNMT3L Homo sapiens Q9UJW3
Y2H Prey Pooling
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
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

Shwachman-Diamond Syndrome 1

Shwachman-Diamond Syndrome

Shwachman Syndrome

Shwachman-Bodian-Diamond Syndrome

Sds

Pancreatic Insufficiency And Bone Marrow Dysfunction

Shwachman-Bodian Syndrome

SDS1

Lipomatosis Of Pancreas, Congenital

Congenital Lipomatosis Of Pancreas

Shwachman-Diamond Type Metaphyseal Dysplasia

Metaphyseal Chondrodysplasia, Shwachman Type

Shwachman-Diamond-Oski 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
Rattus norvegicus RSL24D1 RGD RGD:1309784
Canis familiaris RSL24D1 VGNC VGNC:45776
Bos taurus RSL24D1 VGNC VGNC:34181
Mus musculus RSL24D1 MGD MGI:2681840
Macaca mulatta RSL24D1 VGNC VGNC:99234
Felis catus RSL24D1 VGNC VGNC:104715