Bos taurus Gene: RFC2
Summary
InnateDB Gene IDBG-639934.3
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol RFC2
Gene Name Replication factor C subunit 2
Synonyms
Species Bos taurus
Ensembl Gene ENSBTAG00000018589
Encoded Proteins
Replication factor C subunit 2
Protein Structure
Useful resources Stemformatics EHFPI ImmGen
Entrez Gene
Summary This gene does not have any Entrez summary - the following is the summary from its human ortholog ENSG00000049541:
The elongation of primed DNA templates by DNA polymerase delta and epsilon requires the action of the accessory proteins, proliferating cell nuclear antigen (PCNA) and replication factor C (RFC). RFC, also called activator 1, is a protein complex consisting of five distinct subunits of 145, 40, 38, 37, and 36.5 kD. This gene encodes the 40 kD subunit, which has been shown to be responsible for binding ATP. Deletion of this gene has been associated with Williams syndrome. Alternatively spliced transcript variants encoding distinct isoforms have been described. [provided by RefSeq, Jul 2008]
This gene encodes a member of the activator 1 small subunits family. The elongation of primed DNA templates by DNA polymerase delta and epsilon requires the action of the accessory proteins, proliferating cell nuclear antigen (PCNA) and replication factor C (RFC). Replication factor C, also called activator 1, is a protein complex consisting of five distinct subunits. This gene encodes the 40 kD subunit, which has been shown to be responsible for binding ATP and may help promote cell survival. Disruption of this gene is associated with Williams syndrome. Alternatively spliced transcript variants encoding distinct isoforms have been described. A pseudogene of this gene has been defined on chromosome 2. [provided by RefSeq, Jul 2013]
Gene Information
Type Protein coding
Genomic Location Chromosome 25:33672213-33686223
Strand Forward strand
Band
Transcripts
ENSBTAT00000024740 ENSBTAP00000024740
Interactions
Number of Interactions This gene and/or its encoded proteins are associated with 1 experimentally validated interaction(s) in this database.
They are also associated with 36 interaction(s) predicted by orthology.
Experimentally validated
Total 1 [view]
Protein-Protein 1 [view]
Protein-DNA 0
Protein-RNA 0
DNA-DNA 0
RNA-RNA 0
DNA-RNA 0
Predicted by orthology
Total 36 [view]
Gene Ontology

Molecular Function
Accession GO Term
GO:0000166 nucleotide binding
GO:0003677 DNA binding
GO:0005515 protein binding
GO:0005524 ATP binding
GO:0017111 nucleoside-triphosphatase activity
Biological Process
GO:0006260 DNA replication
Cellular Component
GO:0005634 nucleus
GO:0005663 DNA replication factor C complex
Orthologs
Species
Homo sapiens
Mus musculus
Gene ID
Gene Order
Pathways
NETPATH
REACTOME
S Phase pathway
Gap-filling DNA repair synthesis and ligation in TC-NER pathway
Extension of Telomeres pathway
Transcription-coupled NER (TC-NER) pathway
DNA Replication pathway
Telomere Maintenance pathway
Polymerase switching on the C-strand of the telomere pathway
Leading Strand Synthesis pathway
Nucleotide Excision Repair pathway
Cell Cycle, Mitotic pathway
Gap-filling DNA repair synthesis and ligation in GG-NER pathway
Global Genomic NER (GG-NER) pathway
Telomere C-strand (Lagging Strand) Synthesis pathway
Synthesis of DNA pathway
Cell Cycle pathway
DNA Repair pathway
Lagging Strand Synthesis pathway
Chromosome Maintenance pathway
G2/M Checkpoints pathway
Activation of ATR in response to replication stress pathway
Polymerase switching pathway
Repair synthesis of patch ~27-30 bases long by DNA polymerase pathway
Cell Cycle Checkpoints pathway
Repair synthesis for gap-filling by DNA polymerase in TC-NER pathway
DNA strand elongation pathway
KEGG
INOH
PID NCI
Pathway Predictions based on Human Orthology Data
NETPATH
REACTOME
Activation of ATR in response to replication stress pathway
Polymerase switching on the C-strand of the telomere pathway
Telomere C-strand (Lagging Strand) Synthesis pathway
Polymerase switching pathway
Leading Strand Synthesis pathway
Repair synthesis for gap-filling by DNA polymerase in TC-NER pathway
Gap-filling DNA repair synthesis and ligation in TC-NER pathway
Transcription-coupled NER (TC-NER) pathway
Repair synthesis of patch ~27-30 bases long by DNA polymerase pathway
Gap-filling DNA repair synthesis and ligation in GG-NER pathway
DNA Replication pathway
Synthesis of DNA pathway
S Phase pathway
Chromosome Maintenance pathway
G2/M Checkpoints pathway
Global Genomic NER (GG-NER) pathway
Telomere Maintenance pathway
Cell Cycle pathway
Cell Cycle, Mitotic pathway
DNA strand elongation pathway
Extension of Telomeres pathway
Lagging Strand Synthesis pathway
Nucleotide Excision Repair pathway
DNA Repair pathway
Cell Cycle Checkpoints pathway
Transcription-coupled NER (TC-NER) pathway
Cell Cycle, Mitotic pathway
Gap-filling DNA repair synthesis and ligation in TC-NER pathway
Chromosome Maintenance pathway
Synthesis of DNA pathway
DNA strand elongation pathway
Repair synthesis for gap-filling by DNA polymerase in TC-NER pathway
DNA Replication pathway
Global Genomic NER (GG-NER) pathway
Gap-filling DNA repair synthesis and ligation in GG-NER pathway
Telomere Maintenance pathway
Cell Cycle pathway
Nucleotide Excision Repair pathway
Cell Cycle Checkpoints pathway
Repair synthesis of patch ~27-30 bases long by DNA polymerase pathway
DNA Repair pathway
Leading Strand Synthesis pathway
Telomere C-strand (Lagging Strand) Synthesis pathway
G2/M Checkpoints pathway
Extension of Telomeres pathway
Polymerase switching pathway
Activation of ATR in response to replication stress pathway
Lagging Strand Synthesis pathway
Polymerase switching on the C-strand of the telomere pathway
S Phase pathway
KEGG
DNA replication pathway
Nucleotide excision repair pathway
Mismatch repair pathway
DNA replication pathway
Nucleotide excision repair pathway
Mismatch repair pathway
INOH
PID NCI
Fanconi anemia pathway
ATR signaling pathway
Cross-References
SwissProt Q05B83
TrEMBL
UniProt Splice Variant
Entrez Gene 508652
UniGene Bt.35362
RefSeq NM_001080903
HUGO
OMIM
CCDS
HPRD
IMGT
EMBL BC122635
GenPept AAI22636
RNA Seq Atlas 508652