U.S. flag

An official website of the United States government

Format

Send to:

Choose Destination

Links from Nucleotide

    • Showing Current items.

    RFC5 replication factor C subunit 5 [ Homo sapiens (human) ]

    Gene ID: 5985, updated on 3-Nov-2024

    Summary

    Official Symbol
    RFC5provided by HGNC
    Official Full Name
    replication factor C subunit 5provided by HGNC
    Primary source
    HGNC:HGNC:9973
    See related
    Ensembl:ENSG00000111445 MIM:600407; AllianceGenome:HGNC:9973
    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
    RFC36
    Summary
    This gene encodes the smallest subunit of the replication factor C complex, which consists of five distinct subunits (140, 40, 38, 37, and 36 kDa) and is required for DNA replication. This subunit interacts with the C-terminal region of proliferating cell nuclear antigen and is required to open and load proliferating cell nuclear antigen onto DNA during S phase. It is a member of the AAA+ (ATPases associated with various cellular activities) ATPase family and forms a core complex with the 38 and 40 kDa subunits that possesses DNA-dependent ATPase activity. A related pseudogene has been identified on chromosome 9. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Nov 2016]
    Expression
    Ubiquitous expression in brain (RPKM 10.5), thyroid (RPKM 6.7) and 25 other tissues See more
    Orthologs
    NEW
    Try the new Gene table
    Try the new Transcript table

    Genomic context

    See RFC5 in Genome Data Viewer
    Location:
    12q24.23
    Exon count:
    16
    Annotation release Status Assembly Chr Location
    RS_2024_08 current GRCh38.p14 (GCF_000001405.40) 12 NC_000012.12 (118016703..118041448)
    RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) 12 NC_060936.1 (118003997..118021853)
    RS_2024_09 previous assembly GRCh37.p13 (GCF_000001405.25) 12 NC_000012.11 (118454508..118470039)

    Chromosome 12 - NC_000012.12Genomic Context describing neighboring genes Neighboring gene uncharacterized LOC105370012 Neighboring gene Sharpr-MPRA regulatory region 11046 Neighboring gene kinase suppressor of ras 2 Neighboring gene H3K27ac hESC enhancer GRCh37_chr12:118021615-118022115 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr12:118066292-118066792 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr12:118066793-118067293 Neighboring gene H3K27ac hESC enhancer GRCh37_chr12:118078225-118078724 Neighboring gene uncharacterized LOC105370011 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr12:118274024-118274569 Neighboring gene OCT4-NANOG-H3K4me1 hESC enhancer GRCh37_chr12:118284773-118285290 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr12:118312867-118313667 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 4918 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 4919 Neighboring gene ReSE screen-validated silencer GRCh37_chr12:118442171-118442363 Neighboring gene MPRA-validated peak1990 silencer Neighboring gene Neanderthal introgressed variant-containing enhancer experimental_24987 Neighboring gene Neanderthal introgressed variant-containing enhancer experimental_24992 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 4920 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 7105 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 7106 Neighboring gene MED14-independent group 3 enhancer GRCh37_chr12:118489679-118490878 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 4921 Neighboring gene uncharacterized LOC124903030 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr12:118523172-118523714 Neighboring gene uncharacterized LOC124903029 Neighboring gene WD repeat and SOCS box containing 2 Neighboring gene V-set and immunoglobulin domain containing 10

    Genomic regions, transcripts, and products

    Expression

    • Project title: HPA RNA-seq normal tissues HPA RNA-seq normal tissues
    • Description: RNA-seq was performed of tissue samples from 95 human individuals representing 27 different tissues in order to determine tissue-specificity of all protein-coding genes
    • BioProject: PRJEB4337
    • Publication: PMID 24309898
    • Analysis date: Wed Apr 4 07:08:55 2018

    Bibliography

    GeneRIFs: Gene References Into Functions

    What's a GeneRIF?

    Phenotypes

    EBI GWAS Catalog

    Description
    Novel genetic loci identified for the pathophysiology of childhood obesity in the Hispanic population.
    EBI GWAS Catalog

    HIV-1 interactions

    Protein interactions

    Protein Gene Interaction Pubs
    Tat tat HIV-1 Tat interacts with the RNA polymerase II holoenzyme, which includes RFC, during Tat-mediated transactivation of the HIV-1 LTR PubMed

    Go to the HIV-1, Human Interaction Database

    Pathways from PubChem

    Interactions

    Products Interactant Other Gene Complex Source Pubs Description

    General gene information

    Markers

    Clone Names

    • MGC1155

    Gene Ontology Provided by GOA

    Function Evidence Code Pubs
    enables ATP binding IEA
    Inferred from Electronic Annotation
    more info
     
    enables ATP hydrolysis activity IEA
    Inferred from Electronic Annotation
    more info
     
    enables DNA binding IEA
    Inferred from Electronic Annotation
    more info
     
    contributes_to DNA clamp loader activity IBA
    Inferred from Biological aspect of Ancestor
    more info
     
    contributes_to DNA clamp loader activity IDA
    Inferred from Direct Assay
    more info
    PubMed 
    enables enzyme binding NAS
    Non-traceable Author Statement
    more info
    PubMed 
    enables protein binding IPI
    Inferred from Physical Interaction
    more info
    PubMed 
    contributes_to single-stranded DNA helicase activity IDA
    Inferred from Direct Assay
    more info
    PubMed 
    Process Evidence Code Pubs
    involved_in DNA duplex unwinding IEA
    Inferred from Electronic Annotation
    more info
     
    involved_in DNA repair IBA
    Inferred from Biological aspect of Ancestor
    more info
     
    involved_in DNA repair NAS
    Non-traceable Author Statement
    more info
    PubMed 
    involved_in DNA replication NAS
    Non-traceable Author Statement
    more info
    PubMed 
    involved_in DNA-templated DNA replication IBA
    Inferred from Biological aspect of Ancestor
    more info
     
    involved_in DNA-templated DNA replication IDA
    Inferred from Direct Assay
    more info
    PubMed 
    involved_in positive regulation of DNA-directed DNA polymerase activity IDA
    Inferred from Direct Assay
    more info
    PubMed 
    Component Evidence Code Pubs
    part_of Ctf18 RFC-like complex IDA
    Inferred from Direct Assay
    more info
    PubMed 
    part_of DNA replication factor C complex IBA
    Inferred from Biological aspect of Ancestor
    more info
     
    part_of DNA replication factor C complex IDA
    Inferred from Direct Assay
    more info
    PubMed 
    part_of DNA replication factor C complex IPI
    Inferred from Physical Interaction
    more info
    PubMed 
    located_in nucleoplasm TAS
    Traceable Author Statement
    more info
     
    is_active_in nucleus IBA
    Inferred from Biological aspect of Ancestor
    more info
     

    General protein information

    Preferred Names
    replication factor C subunit 5
    Names
    A1 36 kDa subunit
    RF-C 36 kDa subunit
    RFC, 36.5 kD subunit
    replication factor C (activator 1) 5, 36.5kDa
    replication factor C, 36-kDa subunit

    NCBI Reference Sequences (RefSeq)

    NEW Try the new Transcript table

    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.

    mRNA and Protein(s)

    1. NM_001130112.4NP_001123584.1  replication factor C subunit 5 isoform 3

      Status: REVIEWED

      Description
      Transcript Variant: This variant (4) differs in the 5' UTR and uses a downstream in-frame start codon, compared to variant 1. The resulting isoform (3) is shorter at the N-terminus, compared to isoform 1.
      Source sequence(s)
      AU121576, BC001866
      UniProtKB/TrEMBL
      A8K4Z2
      Conserved Domains (1) summary
      cl25702
      Location:3244
      Rad17; Rad17 cell cycle checkpoint protein
    2. NM_001130113.3NP_001123585.1  replication factor C subunit 5 isoform 2

      Status: REVIEWED

      Description
      Transcript Variant: This variant (3) differs in the 5' UTR and 5' coding region, and uses an alternate start codon, compared to variant 1. The resulting isoform (2) has a distinct and shorter N-terminus, compared to isoform 1. Variants 2 and 3 encode the same isoform (2).
      Source sequence(s)
      AK094575, BC001866, DB270923
      UniProtKB/TrEMBL
      A8K3S0, Q6LES9
      Conserved Domains (1) summary
      cl25702
      Location:2308
      Rad17; Rad17 cell cycle checkpoint protein
    3. NM_001206801.3NP_001193730.1  replication factor C subunit 5 isoform 4

      See identical proteins and their annotated locations for NP_001193730.1

      Status: REVIEWED

      Description
      Transcript Variant: This variant (5) uses an alternate in-frame splice site in the coding region, compared to variant 1. The resulting isoform (4) is shorter than isoform 1.
      Source sequence(s)
      AB208992, AI567945, AU121576
      UniProtKB/TrEMBL
      A8K3S0, Q6LES9
      Conserved Domains (4) summary
      cd00009
      Location:35176
      AAA; The AAA+ (ATPases Associated with a wide variety of cellular Activities) superfamily represents an ancient group of ATPases belonging to the ASCE (for additional strand, catalytic E) division of the P-loop NTPase fold. The ASCE division also includes ABC, ...
      PRK00440
      Location:16326
      rfc; replication factor C small subunit; Reviewed
      pfam08542
      Location:258324
      Rep_fac_C; Replication factor C C-terminal domain
      pfam16193
      Location:192220
      AAA_assoc_2; AAA C-terminal domain
    4. NM_001346815.2NP_001333744.1  replication factor C subunit 5 isoform 5

      Status: REVIEWED

      Description
      Transcript Variant: This variant (6) differs in the 5' UTR, uses an alternate in-frame splice site in the coding region, and intitiates translation at a downstream in-frame start codon, compared to variant 1. The resulting isoform (5) is shorter than isoform 1.
      Source sequence(s)
      AC131159, AI567945
      UniProtKB/TrEMBL
      A8K4Z2
    5. NM_007370.7NP_031396.1  replication factor C subunit 5 isoform 1

      See identical proteins and their annotated locations for NP_031396.1

      Status: REVIEWED

      Description
      Transcript Variant: This variant (1) encodes the longest isoform (1).
      Source sequence(s)
      AU121576, BC001866
      Consensus CDS
      CCDS9185.1
      UniProtKB/Swiss-Prot
      A8MZ62, B3KSX8, P40937
      UniProtKB/TrEMBL
      A8K3S0, Q6LES9
      Related
      ENSP00000408295.2, ENST00000454402.7
      Conserved Domains (1) summary
      PRK00440
      Location:16329
      rfc; replication factor C small subunit; Reviewed
    6. NM_181578.5NP_853556.2  replication factor C subunit 5 isoform 2

      See identical proteins and their annotated locations for NP_853556.2

      Status: REVIEWED

      Description
      Transcript Variant: This variant (2) differs in the 5' UTR and 5' coding region, and uses an alternate start codon, compared to variant 1. The resulting isoform (2) has a distinct and shorter N-terminus, compared to isoform 1. Variants 2 and 3 encode the same isoform (2).
      Source sequence(s)
      AC131159, AK094575, AU121576, BC001866
      Consensus CDS
      CCDS41843.2
      UniProtKB/TrEMBL
      A8K3S0, Q6LES9
      Related
      ENSP00000376325.2, ENST00000392542.6
      Conserved Domains (1) summary
      cl25702
      Location:2308
      Rad17; Rad17 cell cycle checkpoint protein

    RNA

    1. NR_144504.2 RNA Sequence

      Status: REVIEWED

      Description
      Transcript Variant: This variant (7) uses an alternate splice site in an internal exon, compared to variant 1. This variant is represented as non-coding because the use of the 5'-most expected translational start codon, as used in variant 1, renders the transcript a candidate for nonsense-mediated mRNA decay (NMD).
      Source sequence(s)
      AC131159, AI567945

    RefSeqs of Annotated Genomes: GCF_000001405.40-RS_2024_08

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

    Reference GRCh38.p14 Primary Assembly

    Genomic

    1. NC_000012.12 Reference GRCh38.p14 Primary Assembly

      Range
      118016703..118041448
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    RNA

    1. XR_007063112.1 RNA Sequence

    2. XR_007063111.1 RNA Sequence

    3. XR_007063113.1 RNA Sequence

    Alternate T2T-CHM13v2.0

    Genomic

    1. NC_060936.1 Alternate T2T-CHM13v2.0

      Range
      118003997..118021853
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    RNA

    1. XR_008488659.1 RNA Sequence

    2. XR_008488660.1 RNA Sequence