1. Gene
  2. RPS14 - ribosomal protein S14 Gene

RPS14 - ribosomal protein S14 Gene

中文名称:核糖体蛋白 S14

种属: Homo sapiens

同用名: S14; EMTB

基因 ID: 6208 | 基因类型: protein coding

关于 RPS14

Cytogenetic location: 5q33.1 Genomic coordinates (GRCh38): 5:150,442,635-150,449,739 (from NCBI)

This gene has 8 transcripts (splice variants), 272 orthologues, 1 paralogue and is associated with 2 phenotypes. Ubiquitous expression in ovary (RPKM 306.3), bone marrow (RPKM 258.9) 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的 S11P 家族。它位于细胞质中。文献中已经描述了利用替代转录起始位点的转录变体。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。在中国仓鼠卵巢细胞中,该基因的突变可导致对蛋白质合成抑制剂依米丁的耐药性。已为该基因发现了编码相同蛋白质的多个可变剪接转录物变体。[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 S11P family of ribosomal proteins. It is located in the cytoplasm. Transcript variants utilizing alternative transcription initiation sites have been described in the literature. As is typical for genes encoding ribosomal proteins, there are multiple processed pseudogenes of this gene dispersed through the genome. In Chinese hamster ovary cells, mutations in this gene can lead to resistance to emetine, a protein synthesis inhibitor. Multiple alternatively spliced transcript variants encoding the same protein have been found for this gene. [provided by RefSeq, Jul 2008]

RPS14 基因产物(3)

mRNA Protein Name
NM_001025070.2 NP_001020241.1 40S ribosomal protein S14
NM_001025071.2 NP_001020242.1 40S ribosomal protein S14
NM_005617.4 NP_005608.1 40S ribosomal protein S14
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 mRNA 5'-UTR binding IDA
IDA: 通过直接分析推断
7867928 GOA
enables protein binding IPI
IPI: 通过物理相互作用推断
16189514 GOA
enables structural constituent of ribosome IDA
IDA: 通过直接分析推断
23636399 GOA
enables translation regulator activity IMP
IMP: 通过突变表型推断
3683397 GOA
生物过程 GO 注释 逻辑证据 参考文献 来源
involved in cytoplasmic translation IMP
IMP: 通过突变表型推断
9152021 GOA
involved in erythrocyte differentiation IMP
IMP: 通过突变表型推断
18202658 GOA
involved in negative regulation of transcription by RNA polymerase II IDA
IDA: 通过直接分析推断
7867928 GOA
involved in ribosomal small subunit biogenesis IDA
IDA: 通过直接分析推断
34516797 GOA
involved in translation IMP
IMP: 通过突变表型推断
3683397 GOA
细胞组分 GO 注释 逻辑证据 参考文献 来源
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
located in nucleolus IDA
IDA: 通过直接分析推断
9152021 GOA
is active in postsynaptic density EXP
EXP: 通过实验结果推断
21170055 GOA
is active in postsynaptic density IDA
IDA: 通过直接分析推断
21170055 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

RPS14 蛋白结构

Ribosomal_S11

Ribosomal_S11: Ribosomal protein S11 (29 - 147)

  • 0
  • 100
  • 151 a.a.
蛋白主名 其他名称

40S ribosomal protein S14

emetine resistance

RPS14 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
RPS14 P62263 AK6 Homo sapiens Q9Y3D8
Validated Y2H
25416956
种属内
RPS14 P62263 AK6 Homo sapiens Q9Y3D8
Anti Tag CoIP
28514442
种属内
RPS14 P62263 RPS3A Homo sapiens P61247
Anti Tag CoIP
33961781
种属内
RPS14 P62263 RPS3A Homo sapiens P61247
Anti Tag CoIP
28514442
种属内
RPS14 P62263 TAF9 Homo sapiens Q16594
Y2H Array
16713569
种属内
RPS14 P62263 TAF9 Homo sapiens Q16594
Anti Tag CoIP
33961781
种属内
RPS14 P62263 TAF9 Homo sapiens Q16594
Y2H Pooling
16189514
种属内
RPS14 P62263 KRR1 Homo sapiens Q13601
Validated Y2H
32296183
种属内
RPS14 P62263 KRR1 Homo sapiens Q13601
Anti Tag CoIP
33961781
种属内
RPS14 P62263 KRR1 Homo sapiens Q13601
Y2H Array
32296183
种属内
RPS14 P62263 KRR1 Homo sapiens Q13601
Anti Tag CoIP
28514442
种属内
RPS14 P62263 KRR1 Homo sapiens Q13601
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
Chromosome 5q Deletion Syndrome

5q- Syndrome

Mar

Myelodysplastic Syndrome Associated With Isolated Del Chromosome Abnormality

Macrocytic Anemia, Refractory, Due To 5q Deletion, Somatic

5q Deletion Syndrome

5q Minus Syndrome

Refractory Macrocytic Anemia Due To 5q Deletion

Myelodysplastic Syndrome With Isolated Del

Macrocytic Anemia, Refractory, Due To 5q Deletion

5q- Syndrome, Refractory Macrocytic Anemia Due To 5q Deletion

5q Syndrome

Chromosome 5q Deletion

Myelodysplastic Syndrome With 5q Deletion

Myelodysplastic Syndrome With 5q Deletion Syndrome

Anemia, Macrocytic, Refractory, Due To 5q Deletion, Somatic

5q-Syndrome

Chromosome 5, Trisomy 5q

Loss Of Chromosome 5q

5 Q- Syndrome

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

Dyskeratosis Congenita, X-Linked

DKCX

X-Linked Dyskeratosis Congenita

Zinsser-Cole-Engman Syndrome

Hoyeraal-Hreidarsson Syndrome

Dyskeratosis Congenita X-Linked

HHS

Cerebellar Hypoplasia With Pancytopenia

Prenatal Growth Retardation With Progressive Pancytopenia And Cerebellar Hypoplasia

Dyskeratosis Congenita

Retinitis Pigmentosa 14

RP14

Retinitis Pigmentosa Juvenile Tulp1-Related

Retinitis Pigmentosa-14

Retinitis Pigmentosa, Type 14

Cartilage-Hair Hypoplasia

Metaphyseal Chondrodysplasia, Mckusick Type

CHH

Mckusick Type Metaphyseal Chondrodysplasia

Metaphyseal Dysplasia Without Hypotrichosis

Cartilage Hair Hypoplasia Like Syndrome

Metaphyseal Chondrodysplasia Mckusick Type

Chhv

Cartilage-Hair Hypoplasia Variant, Skeletal Manifestations Only

Cartilage-Hair Hypoplasia-Like Skeletal Dysplasia Without Hypotrichosis Or Immunodeficiency

Cartilage-Hair Syndrome

Mckusick'S Metaphyseal Chondrodysplasia Syndrome

Metaphyseal Chondrodysplasia, Recessive Type

Autosomal Recessive Metaphyseal Chondrodysplasia

Macrocytic Anemia

Anemia Macrocytic

Anemia, Macrocytic

Macrocytic Anaemia

Bowen-Conradi Syndrome

BWCNS

Bowen Hutterite Syndrome

Bowen-Conradi Hutterite Syndrome

Bowen Syndrome, Hutterite Type

Bowen Hutterite Syndrome, Formerly

Hutterite Syndrome

Bowen Syndrome Hutterite Type

Fetal Growth Retardation

Treacher Collins Syndrome 1

Treacher Collins Syndrome

Mandibulofacial Dysostosis

Treacher Collins-Franceschetti Syndrome

Tcof

Tcs

Mfd1

Franceschetti-Klein Syndrome

TCS1

Franceschetti Syndrome

Franceschetti-Zwahlen-Klein Syndrome

Zygoauromandibular Dysplasia

Treacher-Collins Syndrome

Mandibulofacial Dysostosis Without Limb Anomalies

Bilateral And Symmetric Oto-Mandibular Dysplasia

Anauxetic Dysplasia 1

Anauxetic Dysplasia

Spondylometaepiphyseal Dysplasia, Menger Type

Spondylometaepiphyseal Dysplasia, Anauxetic Type

Spondyloepimetaphyseal Dysplasia, Anauxetic Type

ANXD1

Anxd

Spondylometaepiphyseal Dysplasia Anauxetic Type

Spondylometaepiphyseal Dysplasia Menger Type

Ad

Spondyloepimetaphyseal Dysplasia, Menger Type

Dysplasia, Anauxetic, Type 1

Dyskeratosis Congenita

Dyskeratosis Congenita Autosomal Dominant

Dc

Dkc

Zinsser-Engman-Cole Syndrome

Dyskeratosis Congenita, Autosomal Dominant

Autosomal Dominant Dyskeratosis Congenita

Dkca

Dyskeratosis Congenita Scoggins Type

Zinsser-Cole-Engman Syndrome

X-Linked Dyskeratosis Congenita

Hoyeraal-Hreidarsson Syndrome

Thrombocytopenia

Low Platelet Count

Low Platelets

Decreased Platelets

Platelet Dysfunction Nos

Aplastic Anemia

Aplastic Anemia, Susceptibility To

Anemia Aplastic

Idiopathic Aplastic Anemia

Secondary Aplastic Anemia

Idiopathic Bone Marrow Failure

Aplastic Anemia Idiopathic

AA

Anemia, Aplastic

Aplastic Anemia, Idiopathic

Erythroid Aplasia

Aa - [Aplastic Anaemia]

Haematopoietic Aplasia

Aleukia Haemorrhagica

Anaemia Due To Decreased Red Cell Production

Aplasia Bone Marrow

Aplastic Bone Marrow

Hypoplastic Anaemia Nos

Myeloid Bone Marrow Aplasia

Pancytopenia

Panhaematopenia

Hypoproliferative Anaemia

Medullary Hypoplasia

Red Blood Cells Hypoplastic Anaemia

Panmyelophthisis

Panhemocytopenia

Refractive Hypoproliferative Anaemia

Toxic Anaemia

Toxic Aplastic Anaemia

Aplastic Anaemia Due To Toxic Cause

Idiopathic Aplastic Anaemia Nos

Myelodysplastic Syndrome

Myelodysplastic Syndromes

Myelodysplasia

MDS

Myelodysplastic Syndrome Included

Myelodysplastic Syndrome, Susceptibility To, Included

Myelodysplastic Syndrome, Somatic

Myelodysplastic Syndrome, Susceptibility To

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
Felis catus RPS14 VGNC VGNC:64751
Rattus norvegicus RPS14 RGD RGD:62025
Macaca mulatta RPS14 VGNC VGNC:76926
Mus musculus RPS14 MGD MGI:98107