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    RPS10 ribosomal protein S10 [ Homo sapiens (human) ]

    Gene ID: 6204, updated on 5-May-2013
    Official Symbol
    RPS10provided by HGNC
    Official Full Name
    ribosomal protein S10provided by HGNC
    Primary source
    HGNC:10383
    Locus tag
    RP11-375E1__A.4
    See related
    Ensembl:ENSG00000124614; HPRD:04697; MIM:603632; Vega:OTTHUMG00000014546
    Gene type
    protein coding
    RefSeq status
    REVIEWED
    Organism
    Homo sapiens
    Lineage
    Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
    Also known as
    S10; DBA9
    Summary
    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 S10E family of ribosomal proteins. It is located in the cytoplasm. Variable expression of this gene in colorectal cancers compared to adjacent normal tissues has been observed, although no correlation between the level of expression and the severity of the disease has been found. As is typical for genes encoding ribosomal proteins, there are multiple processed pseudogenes of this gene dispersed through the genome. Alternate splicing results in multiple transcript variants that encode the same protein. Naturally occurring read-through transcription occurs between this locus and the neighboring locus NUDT3 (nudix (nucleoside diphosphate linked moiety X)-type motif 3).[provided by RefSeq, Feb 2011]
    Location :
    6p21.31
    Sequence :
    Chromosome: 6; NC_000006.11 (34385231..34393902, complement)
    See RPS10 in Epigenomics, MapViewer

    Chromosome 6 - NC_000006.11Genomic Context describing neighboring genes Neighboring gene ribosomal protein L35 pseudogene 2 Neighboring gene RPS10-NUDT3 readthrough Neighboring gene nudix (nucleoside diphosphate linked moiety X)-type motif 3 Neighboring gene protein kinase C and casein kinase substrate in neurons 1 Neighboring gene SAM pointed domain containing ets transcription factor

    GeneRIFs: Gene References Into Functions What's a GeneRIF?

    Diamond-Blackfan anemia 9

    Summary from GeneReviews: Diamond-Blackfan Anemia Go to GeneReviews

    Disease Characteristics
    Diamond-Blackfan anemia (DBA) in its classic form is characterized by a profound isolated normochromic and usually macrocytic anemia with normal leukocytes and platelets, congenital malformations in approximately 50% of affected individuals, and growth retardation in 30% of affected individuals. The hematologic complications occur in 90% of affected individuals during the first year of life (median age of onset is two months). Eventually, 40% of affected individuals are corticosteroid dependent, 40% are transfusion dependent, and 20% go into remission. The phenotypic spectrum ranges from a mild form (e.g., mild anemia; no anemia with only subtle erythroid abnormalities; physical malformations without anemia) to a severe form of fetal anemia resulting in non-immune hydrops fetalis. DBA is associated with an increased risk of acute myelogenous leukemia (AML), myelodysplastic syndrome (MDS), and solid tumors including osteogenic sarcoma.
    Diagnosis Testing
    The diagnosis is based on the presence of: normochromic, usually macrocytic, anemia; reticulocytopenia; normal or slightly decreased leukocyte counts; normal or increased platelet counts; and normocellular bone marrow with selective deficiency of red cell precursors. Other genetic forms of anemia, such as Fanconi anemia, need to be considered and ruled out as appropriate. DBA has been associated with mutations in nine genes that encode ribosomal proteins. A mutation in one of these nine genes is identified in approximately 53% of individuals with DBA. Such testing is available clinically.
    Genetic Counseling
    DBA is inherited in an autosomal dominant manner. Approximately 40% to 45% of affected individuals have inherited the mutation from a parent; approximately 55% to 60% have a de novo mutation. Each child of an individual with DBA has a 50% chance of inheriting the mutation. Prenatal diagnosis for pregnancies at increased risk is possible if the disease-causing mutation has been identified in the family; if no laboratory offering prenatal testing is listed in the GeneTests Laboratory Directory, such testing may be available through laboratories offering custom mutation prenatal testing.
    References
    Protein Gene Interaction Pubs
    Nef, p27 nef HIV-1 Nef inhibits translation in vitro by interacting with two components of the 40S small ribosomal subunits, the RPS10 protein and the 18S rRNA PubMed

    Go to the HIV-1, Human Protein Interaction Database

    Products Interactant Other Gene Complex Source Pubs Description
    P46783 P54257 HAP1    HPRD  PubMed  
    P46783 O00291 HIP1    HPRD  PubMed  
    P46783 O95251 KAT7    HPRD  PubMed  
    P46783 P35080 PFN2    HPRD  PubMed  
    P46783 O95997 PTTG1    HPRD  PubMed  
    BioGRID:112118 BioGRID:106848 APP    BioGRID  PubMed Reconstituted Complex 
    BioGRID:112118 BioGRID:107021 ATP5O    BioGRID  PubMed Co-fractionation 
    BioGRID:112118 BioGRID:120937 CAND1    BioGRID  PubMed Affinity Capture-MS 
    BioGRID:112118 BioGRID:107358 CD4    BioGRID  PubMed Affinity Capture-MS 
    BioGRID:112118 BioGRID:107452 CDK2    BioGRID  PubMed Affinity Capture-MS 
    BioGRID:112118 BioGRID:116183 COPS5    BioGRID  PubMed Affinity Capture-MS 
    BioGRID:112118 BioGRID:114032 CUL1    BioGRID  PubMed Affinity Capture-MS 
    BioGRID:112118 BioGRID:114030 CUL3    BioGRID  PubMed Affinity Capture-MS 
    BioGRID:112118 BioGRID:113743 CUL5    BioGRID  PubMed Affinity Capture-MS 
    BioGRID:112118 BioGRID:107998 DCC    BioGRID  PubMed Affinity Capture-MS; Affinity Capture-Western 
    BioGRID:112118 BioGRID:119920 DCUN1D1    BioGRID  PubMed Affinity Capture-MS 
    BioGRID:112118 BioGRID:108100 DMPK    BioGRID  PubMed Two-hybrid 
    BioGRID:112118 BioGRID:108126 DNMT3B    BioGRID  PubMed Two-hybrid 
    BioGRID:112118 BioGRID:108190 DVL3    BioGRID  PubMed Two-hybrid 
    BioGRID:112118 BioGRID:114265 EED    BioGRID  PubMed Two-hybrid 
    BioGRID:112118 BioGRID:123822 EIF2A    BioGRID  PubMed Affinity Capture-MS 
    BioGRID:112118 BioGRID:114210 EIF3A    BioGRID  PubMed Affinity Capture-MS 
    BioGRID:112118 BioGRID:109857 EIF3E    BioGRID  PubMed Affinity Capture-MS 
    BioGRID:112118 BioGRID:118148 EIF3K    BioGRID  PubMed Affinity Capture-MS 
    BioGRID:112118 BioGRID:108403 ESR1    BioGRID  PubMed Affinity Capture-MS 
    BioGRID:112118 BioGRID:108621 FN1    BioGRID  PubMed Affinity Capture-MS 
    BioGRID:112118 BioGRID:109268 H2AFX    BioGRID  PubMed Affinity Capture-MS 
    BioGRID:112118 BioGRID:114480 HAP1    BioGRID  PubMed Two-hybrid 
    BioGRID:112118 BioGRID:120968 HDAC8    BioGRID  PubMed Negative Genetic 
    BioGRID:112118 BioGRID:109339 HIP1    BioGRID  PubMed Two-hybrid 
    BioGRID:112118 BioGRID:109883 ITGA4    BioGRID  PubMed Affinity Capture-MS 
    BioGRID:112118 BioGRID:116315 KAT7    BioGRID  PubMed Two-hybrid 
    BioGRID:112118 BioGRID:115114 KIAA0101    BioGRID  PubMed Affinity Capture-MS 
    BioGRID:112118 BioGRID:116947 LARP1    BioGRID  PubMed Affinity Capture-MS 
    BioGRID:112118 BioGRID:110455 MME    BioGRID  PubMed Affinity Capture-MS 
    BioGRID:112118 BioGRID:110484 MOV10    BioGRID  PubMed Co-fractionation 
    BioGRID:112118 BioGRID:110815 NEDD8    BioGRID  PubMed Affinity Capture-MS 
    BioGRID:112118 BioGRID:111238 PFN2    BioGRID  PubMed Two-hybrid 
    BioGRID:112118 BioGRID:111314 PIK3R2    BioGRID  PubMed Affinity Capture-MS 
    BioGRID:112118 BioGRID:120319 PINX1    BioGRID  PubMed Affinity Capture-MS 
    BioGRID:112118 BioGRID:118151 PRPF19    BioGRID  PubMed Co-fractionation 
    BioGRID:112118 BioGRID:114577 PRPF3    BioGRID  PubMed Co-fractionation 
    BioGRID:112118 BioGRID:114576 PRPF4    BioGRID  PubMed Co-fractionation 
    BioGRID:112118 BioGRID:114663 PTTG1    BioGRID  PubMed Affinity Capture-Western; Reconstituted Complex 
    BioGRID:112118 BioGRID:111822 RAD21    BioGRID  PubMed Affinity Capture-Western 
    BioGRID:112118 BioGRID:112054 RPL10    BioGRID  PubMed Co-fractionation 
    BioGRID:112118 BioGRID:126711 RPL10L    BioGRID  PubMed Co-fractionation 
    BioGRID:112118 BioGRID:112055 RPL11    BioGRID  PubMed Co-fractionation 
    BioGRID:112118 BioGRID:114507 RPL14    BioGRID  PubMed Co-fractionation 
    BioGRID:112118 BioGRID:112074 RPL27    BioGRID  PubMed Co-fractionation 
    BioGRID:112118 BioGRID:112077 RPL28    BioGRID  PubMed Affinity Capture-MS 
    BioGRID:112118 BioGRID:112079 RPL31    BioGRID  PubMed Co-fractionation 
    BioGRID:112118 BioGRID:112045 RPL5    BioGRID  PubMed Co-fractionation 
    BioGRID:112118 BioGRID:112053 RPL9    BioGRID  PubMed Co-fractionation 
    BioGRID:112118 BioGRID:112094 RPLP0    BioGRID  PubMed Co-fractionation 
    BioGRID:112118 BioGRID:128652 RPLP0P6    BioGRID  PubMed Co-fractionation 
    BioGRID:112118 BioGRID:112095 RPLP1    BioGRID  PubMed Co-fractionation 
    BioGRID:112118 BioGRID:112119 RPS11    BioGRID  PubMed Affinity Capture-MS; Co-fractionation 
    BioGRID:112118 BioGRID:112120 RPS12    BioGRID  PubMed Affinity Capture-MS 
    BioGRID:112118 BioGRID:112121 RPS13    BioGRID  PubMed Affinity Capture-MS; Co-fractionation 
    BioGRID:112118 BioGRID:112122 RPS14    BioGRID  PubMed Affinity Capture-MS; Co-fractionation 
    BioGRID:112118 BioGRID:112123 RPS15    BioGRID  PubMed Affinity Capture-MS 
    BioGRID:112118 BioGRID:112124 RPS15A    BioGRID  PubMed Affinity Capture-MS; Co-fractionation 
    BioGRID:112118 BioGRID:112131 RPS16    BioGRID  PubMed Affinity Capture-MS; Co-fractionation 
    BioGRID:112118 BioGRID:1527840 RPS17L    BioGRID  PubMed Affinity Capture-MS 
    BioGRID:112118 BioGRID:112136 RPS18    BioGRID  PubMed Affinity Capture-MS 
    BioGRID:112118 BioGRID:112137 RPS19    BioGRID  PubMed Affinity Capture-MS; Co-fractionation 
    BioGRID:112118 BioGRID:112101 RPS2    BioGRID  PubMed Affinity Capture-MS; Co-fractionation 
    BioGRID:112118 BioGRID:112138 RPS20    BioGRID  PubMed Affinity Capture-MS 
    BioGRID:112118 BioGRID:112141 RPS21    BioGRID  PubMed Affinity Capture-MS 
    BioGRID:112118 BioGRID:112142 RPS23    BioGRID  PubMed Affinity Capture-MS 
    BioGRID:112118 BioGRID:112143 RPS24    BioGRID  PubMed Affinity Capture-MS; Co-fractionation 
    BioGRID:112118 BioGRID:112144 RPS25    BioGRID  PubMed Affinity Capture-MS; Co-fractionation 
    BioGRID:112118 BioGRID:112145 RPS26    BioGRID  PubMed Affinity Capture-MS; Co-fractionation 
    BioGRID:112118 BioGRID:112146 RPS27    BioGRID  PubMed Affinity Capture-MS 
    BioGRID:112118 BioGRID:112147 RPS27A    BioGRID  PubMed Co-fractionation 
    BioGRID:112118 BioGRID:112148 RPS28    BioGRID  PubMed Affinity Capture-MS 
    BioGRID:112118 BioGRID:112149 RPS29    BioGRID  PubMed Affinity Capture-MS; Co-fractionation 
    BioGRID:112118 BioGRID:112102 RPS3    BioGRID  PubMed Affinity Capture-MS; Co-fractionation 
    BioGRID:112118 BioGRID:112103 RPS3A    BioGRID  PubMed Affinity Capture-MS; Co-fractionation 
    BioGRID:112118 BioGRID:112105 RPS4X    BioGRID  PubMed Affinity Capture-MS; Co-fractionation; Reconstituted Complex 
    BioGRID:112118 BioGRID:112107 RPS5    BioGRID  PubMed Affinity Capture-MS 
    BioGRID:112118 BioGRID:112108 RPS6    BioGRID  PubMed Affinity Capture-MS 
    BioGRID:112118 BioGRID:112115 RPS7    BioGRID  PubMed Affinity Capture-MS; Co-fractionation 
    BioGRID:112118 BioGRID:112116 RPS8    BioGRID  PubMed Affinity Capture-MS; Co-fractionation 
    BioGRID:112118 BioGRID:112117 RPS9    BioGRID  PubMed Affinity Capture-MS 
    BioGRID:112118 BioGRID:110115 RPSA    BioGRID  PubMed Co-fractionation 
    BioGRID:112118 BioGRID:117571 SERBP1    BioGRID  PubMed Affinity Capture-MS 
    BioGRID:112118 BioGRID:116983 SIRT1    BioGRID  PubMed Negative Genetic 
    BioGRID:112118 BioGRID:119602 SIRT7    BioGRID  PubMed Affinity Capture-MS 
    BioGRID:112118 BioGRID:121411 SMURF1    BioGRID  PubMed Affinity Capture-MS 
    BioGRID:112118 BioGRID:112497 SUMO2    BioGRID  PubMed Affinity Capture-MS 
    BioGRID:112118 BioGRID:112717 SYK    BioGRID  PubMed Two-hybrid 
    BioGRID:112118 BioGRID:116629 TCF25    BioGRID  PubMed Two-hybrid 
    BioGRID:112118 BioGRID:119995 TMCO1    BioGRID  PubMed Co-fractionation 
    BioGRID:112118 BioGRID:113010 TP53    BioGRID  PubMed Two-hybrid 
    BioGRID:112118 BioGRID:120842 TSR1    BioGRID  PubMed Affinity Capture-MS 
    BioGRID:112118 BioGRID:113164 UBC    BioGRID  PubMed Affinity Capture-MS 
    BioGRID:112118 BioGRID:113885 UBL4A    BioGRID  PubMed Affinity Capture-MS 
    BioGRID:112118 BioGRID:113227 UQCRB    BioGRID  PubMed Co-fractionation 
    BioGRID:112118 BioGRID:113255 VCAM1    BioGRID  PubMed Affinity Capture-MS 
    BioGRID:112118 BioGRID:124031 WIBG    BioGRID  PubMed Affinity Capture-MS 
    BioGRID:112118 BioGRID:121845 WIZ    BioGRID  PubMed Two-hybrid 
    BioGRID:112118 BioGRID:108822 XRCC6    BioGRID  PubMed Two-hybrid 

    Markers

    Homology

    Clone Names

    • MGC88819

    Gene Ontology Provided by GOA

    Function Evidence Code Pubs
    protein binding IPI
    Inferred from Physical Interaction
    more info
     
    Process Evidence Code Pubs
    RNA metabolic process TAS
    Traceable Author Statement
    more info
     
    SRP-dependent cotranslational protein targeting to membrane TAS
    Traceable Author Statement
    more info
     
    cellular protein metabolic process TAS
    Traceable Author Statement
    more info
     
    gene expression TAS
    Traceable Author Statement
    more info
     
    mRNA metabolic process TAS
    Traceable Author Statement
    more info
     
    nuclear-transcribed mRNA catabolic process, nonsense-mediated decay TAS
    Traceable Author Statement
    more info
     
    translation IC
    Inferred by Curator
    more info
    PubMed 
    translation TAS
    Traceable Author Statement
    more info
     
    translational elongation TAS
    Traceable Author Statement
    more info
     
    translational initiation TAS
    Traceable Author Statement
    more info
     
    translational termination TAS
    Traceable Author Statement
    more info
     
    viral infectious cycle TAS
    Traceable Author Statement
    more info
     
    viral reproduction TAS
    Traceable Author Statement
    more info
     
    viral transcription TAS
    Traceable Author Statement
    more info
     
    Component Evidence Code Pubs
    cytosol TAS
    Traceable Author Statement
    more info
     
    cytosolic small ribosomal subunit IDA
    Inferred from Direct Assay
    more info
    PubMed 
    nucleolus IDA
    Inferred from Direct Assay
    more info
     
    ribosome NAS
    Non-traceable Author Statement
    more info
    PubMed 
    Preferred Names
    40S ribosomal protein S10
    Names
    40S ribosomal protein S10

    RefSeqs maintained independently of Annotated Genomes

    These reference sequences exist independently of genome builds. Explain

    These reference sequences are curated independently of the genome annotation cycle, so their versions may not match the RefSeq versions in the current genome build. Identify version mismatches by comparing the version of the RefSeq in this section to the one reported in Genomic regions, transcripts, and products above.

    Genomic

    1. NG_023200.1 RefSeqGene

      Range
      4975..13646
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    mRNA and Protein(s)

    1. NM_001014.4NP_001005.1  40S ribosomal protein S10

      Status: REVIEWED

      Description
      Transcript Variant: This variant (2) differs in the 5' UTR compared to variant 1. Variants 1, 2 and 3 encode the same protein.
      Source sequence(s)
      BC001032, BG940847
      Consensus CDS
      CCDS4792.1
      UniProtKB/Swiss-Prot
      P46783
      Related
      ENSP00000347271, OTTHUMP00000016229, ENST00000326199, OTTHUMT00000040230
      Conserved Domains (1) summary
      pfam03501
      Location:3101
      Blast Score: 491
      S10_plectin; Plectin/S10 domain
    2. NM_001203245.2NP_001190174.1  40S ribosomal protein S10

      Status: REVIEWED

      Description
      Transcript Variant: This variant (1) represents the longer transcript. Variants 1, 2 and 3 encode the same protein.
      Source sequence(s)
      BC071946, BG532491
      Consensus CDS
      CCDS4792.1
      UniProtKB/Swiss-Prot
      P46783
      Conserved Domains (1) summary
      pfam03501
      Location:3101
      Blast Score: 491
      S10_plectin; Plectin/S10 domain
    3. NM_001204091.1NP_001191020.1  40S ribosomal protein S10

      Status: REVIEWED

      Description
      Transcript Variant: This variant (3) differs in the 5' UTR compared to variant 1. Variants 1, 2 and 3 encode the same protein.
      Source sequence(s)
      BU956627, BX255972
      Consensus CDS
      CCDS4792.1
      UniProtKB/Swiss-Prot
      P46783
      Conserved Domains (1) summary
      pfam03501
      Location:3101
      Blast Score: 491
      S10_plectin; Plectin/S10 domain

    RefSeqs of Annotated Genomes: Homo sapiens Annotation Release 104

    The following sections contain reference sequences that belong to a specific genome build. Explain

    Reference GRCh37.p10 Primary Assembly

    Genomic

    1. NC_000006.11 Reference GRCh37.p10 Primary Assembly

      Range
      34385231..34393902, complement
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    Alternate HuRef

    Genomic

    1. AC_000138.1 Alternate HuRef

      Range
      34107972..34116617, complement
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    Alternate CHM1_1.0

    Genomic

    1. NC_018917.1 Alternate CHM1_1.0

      Range
      34300359..34309069, complement
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

      Supplemental Content

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