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  2. RPSA - ribosomal protein SA Gene

RPSA - ribosomal protein SA Gene

中文名称:核糖体蛋白

种属: Homo sapiens

同用名: SA; LBP; LRP; p40; 67LR; ICAS; lamR; 37LRP; LAMBR; LAMR1; LRP/LR; LBP/p40; NEM/1CHD4

基因 ID: 3921 | 基因类型: protein coding

关于 RPSA

Cytogenetic location: 3p22.1 Genomic coordinates (GRCh38): 3:39,406,720-39,412,542 (from NCBI)

This gene has 20 transcripts (splice variants), 211 orthologues, 1 paralogue and is associated with 2 phenotypes. Ubiquitous expression in ovary (RPKM 792.7), lymph node (RPKM 583.0) and 25 other tissues.

功能概要

层粘连蛋白是细胞外基质糖蛋白家族,是基底膜的主要非胶原成分。它们涉及多种生物过程,包括细胞粘附、分化、迁移、信号传导、神经突生长和转移。层粘连蛋白的许多作用是通过与细胞表面受体的相互作用介导的。这些受体包括整合素家族的成员,以及非整合素层粘连蛋白结合蛋白。该基因编码高亲和力、非整联蛋白家族层粘连蛋白受体 1。该受体被称为 67 kD 层粘连蛋白受体、37 kD 层粘连蛋白受体前体 (37LRP) 和 p40 核糖体相关蛋白。层粘连蛋白受体 1 的氨基酸序列在进化过程中高度保守,表明其具有关键的生物学功能。已经观察到层粘连蛋白受体转录物的水平在结肠癌组织和肺癌细胞系中高于它们的正常对应物。此外,该多肽在癌细胞中的上调与其侵袭性和转移性表型之间存在相关性。存在该基因的多个拷贝,但是,它们中的大多数是假基因,被认为是由逆位事件引起的。已经为该基因发现了编码相同蛋白质的两个选择性剪接的转录物变体。[RefSeq 提供,2008 年 7 月]

Laminins, a family of extracellular matrix glycoproteins, are the major noncollagenous constituent of basement membranes. They have been implicated in a wide variety of biological processes including cell adhesion, differentiation, migration, signaling, neurite outgrowth and metastasis. Many of the effects of laminin are mediated through interactions with cell surface receptors. These receptors include members of the Integrin family, as well as non-integrin laminin-binding proteins. This gene encodes a high-affinity, non-integrin family, laminin receptor 1. This receptor has been variously called 67 kD laminin receptor, 37 kD laminin receptor precursor (37LRP) and p40 ribosome-associated protein. The amino acid sequence of laminin receptor 1 is highly conserved through evolution, suggesting a key biological function. It has been observed that the level of the laminin receptor transcript is higher in colon carcinoma tissue and lung Cancer cell line than their normal counterparts. Also, there is a correlation between the upregulation of this polypeptide in Cancer cells and their invasive and metastatic phenotype. Multiple copies of this gene exist, however, most of them are pseudogenes thought to have arisen from retropositional events. Two alternatively spliced transcript variants encoding the same protein have been found for this gene. [provided by RefSeq, Jul 2008]

RPSA 基因产物(2)

mRNA Protein Name
NM_001304288.2 NP_001291217.1 40S ribosomal protein SA isoform 2
NM_002295.6 NP_002286.2 40S ribosomal protein SA isoform 1
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 DNA binding IDA
IDA: 通过直接分析推断
38114488 GOA
enables protein binding IPI
IPI: 通过物理相互作用推断
16169070 GOA
enables ribosome binding IPI
IPI: 通过物理相互作用推断
10079194 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 antiviral innate immune response IDA
IDA: 通过直接分析推断
38114488 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
16263087 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
is active in nucleus IDA
IDA: 通过直接分析推断
38114488 GOA
located in plasma membrane IDA
IDA: 通过直接分析推断
16263087 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

RPSA 蛋白结构

Ribosomal_S2

Ribosomal_S2: Ribosomal protein S2 (19 - 185)

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

40S ribosomal protein SA

37 kDa laminin receptor

RPSA 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
RPSA P08865 CCDC13 Homo sapiens Q8IYE1
Validated Y2H
32296183
种属内
RPSA P08865 KIF1B Homo sapiens O60333-2
Y2H Array
32814053
种属内
RPSA P08865 KIF1B Homo sapiens O60333-2
Y2H Pooling
32814053
种属内
RPSA P08865 KIF1B Homo sapiens O60333-2
Validated Y2H
32814053
种属内
RPSA P08865 HSPB1 Homo sapiens P04792
Y2H Pooling
32814053
种属内
RPSA P08865 HSPB1 Homo sapiens P04792
Validated Y2H
32814053
种属内
RPSA P08865 HSPB1 Homo sapiens P04792
Y2H Array
32814053
种属内
RPSA P08865 HSPB1 Homo sapiens P04792
Reverse RRS
25277244
种属内
RPSA P08865 KARS1 Homo sapiens Q15046
Anti Tag CoIP
24212136
种属内
RPSA P08865 KARS1 Homo sapiens Q15046
Pull Down
24212136
种属内
RPSA P08865 KARS1 Homo sapiens Q15046
NMR
24983501
种属内
RPSA P08865 KARS1 Homo sapiens Q15046
GMS
24983501
种属内
RPSA P08865 KARS1 Homo sapiens Q15046
Y2H
24212136
种属内
RPSA P08865 RPS21 Homo sapiens P63220
Anti Tag CoIP
33961781
种属内
RPSA P08865 RPS21 Homo sapiens P63220
Anti Tag CoIP
28514442
种属内
RPSA P08865 TINF2 Homo sapiens Q9BSI4
Pull Down
21044950
种属内
RPSA P08865 TINF2 Homo sapiens Q9BSI4
BiFC
21044950
种属内
RPSA P08865 WFS1 Homo sapiens O76024
Validated Y2H
32814053
种属内
RPSA P08865 WFS1 Homo sapiens O76024
Y2H Array
32814053
种属内
RPSA P08865 WFS1 Homo sapiens O76024
Y2H Pooling
32814053
种属内
RPSA P08865 GAB2 Homo sapiens Q9UQC2
Validated Y2H
32814053
种属内
RPSA P08865 GAB2 Homo sapiens Q9UQC2
Y2H Array
32814053
种属内
RPSA P08865 GAB2 Homo sapiens Q9UQC2
Y2H Pooling
32814053
种属间: 跨种属相互作用 种属内: 同种属相互作用

RPSA 抗体

目录号 产品名 应用 反应物种
HY-P82214 67kDa Laminin Receptor Antibody (YA1959) WB, IP Human, Mouse, Rat

关联疾病

疾病名称 别名
Asplenia, Isolated Congenital

ICAS

Splenic Hypoplasia

Familial Isolated Congenital Asplenia

Hyposplenia, Isolated Congenital

Asplenia, Familial

Isolated Congenital Asplenia

Congenital Hypoplasia Of Spleen

Hypoplasia Of Spleen

Spenlic Hypoplasia

Congenital Isolated Hyposplenia

Familial Asplenia

Venezuelan Equine Encephalitis

Venezuelan Equine Fever

Venezuelan Equine Encephalomyelitis

Encephalitis Venezuelan Equine

Encephalomyelitis, Venezuelan Equine

Venezuelan Encephalitis

Disorder Due To Venezuelan Equine Encephalitis Virus

Venezuelan Equine Encephalitis Virus Infection

Venezuelan Equine Encephalomyelitis Virus Disease

Encephalitis

Mumps Encephalitis

Mumps Meningoencephalitis

Herpes Simplex Neuroinvasion

Herpetic Encephalitis

Herpetic Encephalopathy

Herpes Simplex Encephalitis, Myelitis Or Encephalomyelitis

Encephalitis Due To Herpesviridae

Encephalitis Due To Herpesvirus

Herpes Encephalitis

Herpesviral Encephalitis

Herpes Simplex Encephalitis

Hsv - [Herpes Simplex Virus] Encephalitis

Herpes Virus Encephalitis

Simian B Disease

Simian B Disorder

Encephalitis Nec

Idiopathic Encephalitis

Dengue Virus

Dengue Virus, Susceptibility To

Dengue Fever, Protection Against

Dengue Fever

Tick-Borne Encephalitis

Siberian Tick-Borne Encephalitis

Encephalitis, Tick-Borne

Central European Encephalitis

Far Eastern Tbe

Russian Spring-Summer Encephalitis

Taiga Encephalitis

West-Siberian Encephalitis

Western European Tick-Borne Encephalitis

Tbe

Encephalitis Tick-Borne

Encephalitis, Central European

Encephalitis, Far Eastern Russian

Scrapie
Creutzfeldt-Jakob Disease

Variant Creutzfeldt-Jakob Disease

CJD

Bovine Spongiform Encephalopathy

Vcjd

Inherited Creutzfeldt-Jakob Disease

Creutzfeldt-Jakob Disease, Familial

Creutzfeldt Jakob Disease

Creutzfeldt-Jacob Disease

Creutzfeldt Jacob Disease

Sporadic Creutzfeldt-Jakob Disease

Encephalopathy, Bovine Spongiform

Creutzfeldt-Jakob Disease, Variant, Resistance To

Creutzfeldt-Jakob Disease, Variant

Creutzfeldt Jacob Syndrome

Jakob-Creutzfeldt Disease

Subacute Spongiform Encephalopathy

Transmissible Virus Dementia

New Variant Of Cjd

Nv-Cjd

Variant Cjd

Variant Creutzfeldt-Jacob Disease

Sporadic Cjd

Inherited Cjd

Acquired Creutzfeldt-Jakob Disease

Variant Mcj

Encephalopathy Bovine Spongiform

Familial Creutzfeldt-Jakob Disease

Creutzfeldt-Jakob Syndrome

New Variant Creutzfeldt-Jakob Disease

Creutzfeldt-Jakob Disease, Sporadic

Acquired Cjd

Scjd - [Sporadic Creutzfeldt-Jakob Disease]

Idiopathic Creutzfeldt-Jakob Disease

Creutzfeld-Jakob Disease Nos

Vcjd - [Variant Creutzfeldt-Jakob Disease]

Flying Phobia

Aerophobia

Prion Disease

Spongiform Encephalopathy

Transmissible Spongiform Encephalopathies

Prion Diseases

Prion Disease Pathway

Transmissible Spongiform Encephalopathy

Prion Induced Disorder

Prion Protein Disease

Inherited Human Transmissible Spongiform Encephalopathies

Prion Protein Diseases

Prion-Associated Disorders

Prion-Induced Disorders

Transmissible Dementias

Tses

Human Prion Disease

Tse

Encephalopathy, Transmissible Spongiform

Prion Disease, Susceptibility To

Spongiform Encephalopathies

Human Transmissible Spongiform Encephalopathies, Inherited

Chronic Wasting Disease

Wasting Disease, Chronic

Gummatous Syphilis
Early Congenital Syphilis
Oral Mucosa Leukoplakia

Leukoplakia, Oral

Leukoplakia Of Buccal Mucosa

Arrhythmogenic Right Ventricular Dysplasia, Familial, 9

Arrhythmogenic Right Ventricular Dysplasia 9

ARVD9

Arrhythmogenic Right Ventricular Cardiomyopathy 9

Arvc9

Familial Arrhythmogenic Right Ventricular Dysplasia 9

Dysplasia, Arrhythmogenic Right Ventricular, Type 9

Meningovascular Neurosyphilis
Primary Syphilis

Early Symptomatic Syphilis

Early Syphilis, Symptomatic

Symptomatic Early Syphilis

Lung Cancer

Lung Carcinoma

Non-Small Cell Lung Carcinoma

Lung Cancer, Susceptibility To

Lung Cancer, Protection Against

Adenocarcinoma Of Lung, Somatic

Adenocarcinoma Of Lung, Response To Tyrosine Kinase Inhibitor In

Nonsmall Cell Lung Cancer

Lung Neoplasm

Carcinoma Of Lung

Lung Non-Small Cell Carcinoma

Non-Small Cell Lung Cancer

Nsclc

Lung Neoplasms

Malignant Neoplasm Of Lung

Alveolar Cell Carcinoma

Nonsmall Cell Lung Cancer, Somatic

Nonsmall Cell Lung Cancer, Response To Tyrosine Kinase Inhibitor In

Nonsmall Cell Lung Cancer, Susceptibility To

Lung Cancer, Somatic

Lung Cancer, Resistance To

Cancer Of Lung

Cancer Of Bronchus

Cancer Of The Lung

Lung Malignancies

Lung Malignant Tumors

Malignant Lung Tumor

Malignant Tumor Of Lung

Pulmonary Cancer

Pulmonary Carcinoma

Pulmonary Neoplasms

Respiratory Carcinoma

LNCR

Adenocarcinoma Of Lung

Neoplasm Of Lung

Cancer Lung

Carcinoma Non-Small Cell Lung

Carcinoma, Non-Small-Cell Lung

Lung Cancers

Lung Carcinomas

Cancer, Lung

Cancer, Lung, Non-Small Cell

Primary Malignant Neoplasm Of Lung

Bronchioloalveolar Adenocarcinoma

Right Atrial Isomerism

Ivemark Syndrome

Asplenia With Cardiovascular Anomalies

RAI

Asplenia Syndrome

Asplenia

Right Isomerism

Splenic Agenesis Syndrome

Bilateral Right-Sidedness Sequence

Right Sided Atrial Isomerism

Isomerism Of Right Atrial Appendage

Heterotaxy, Visceroatrial, Autosomal Recessive

Polyasplenia

Vah, Autosomal Recessive

Atrial Isomerism, Right

Congenital Absence Of Spleen

Bilateral Right-Sidedness

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
Bos taurus RPSA VGNC VGNC:50207
Mus musculus RPSA MGD MGI:105381
Rattus norvegicus RPSA RGD RGD:71026