Bos taurus Gene: LIG1
Summary
InnateDB Gene IDBG-640139.3
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol LIG1
Gene Name DNA ligase 1
Synonyms
Species Bos taurus
Ensembl Gene ENSBTAG00000014595
Encoded Proteins
DNA ligase 1
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 ENSG00000105486:
LIG1 encodes DNA ligase I, with functions in DNA replication and the base excision repair process. Mutations in LIG1 that lead to DNA ligase I deficiency result in immunodeficiency and increased sensitivity to DNA-damaging agents. [provided by RefSeq, Jul 2008]
This gene encodes a member of the ATP-dependent DNA ligase protein family. The encoded protein functions in DNA replication, recombination, and the base excision repair process. Mutations in this gene that lead to DNA ligase I deficiency result in immunodeficiency and increased sensitivity to DNA-damaging agents. Disruption of this gene may also be associated with a variety of cancers. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jan 2014]
Gene Information
Type Protein coding
Genomic Location Chromosome 18:55307590-55334837
Strand Reverse strand
Band
Transcripts
ENSBTAT00000031920 ENSBTAP00000031866
Interactions
Number of Interactions This gene and/or its encoded proteins are associated with 0 experimentally validated interaction(s) in this database.
They are also associated with 6 interaction(s) predicted by orthology.
Predicted by orthology
Total 6 [view]
Gene Ontology

Molecular Function
Accession GO Term
GO:0000166 nucleotide binding
GO:0003677 DNA binding
GO:0003909 DNA ligase activity
GO:0003910 DNA ligase (ATP) activity
GO:0005524 ATP binding
GO:0016874 ligase activity
Biological Process
GO:0006260 DNA replication
GO:0006266 DNA ligation
GO:0006273 lagging strand elongation
GO:0006281 DNA repair
GO:0006303 double-strand break repair via nonhomologous end joining
GO:0006310 DNA recombination
GO:0006974 cellular response to DNA damage stimulus
GO:0042542 response to hydrogen peroxide
GO:0051103 DNA ligation involved in DNA repair
GO:0071897 DNA biosynthetic process
Cellular Component
GO:0005634 nucleus
GO:0005694 chromosome
GO:0005739 mitochondrion
GO:0005794 Golgi apparatus
GO:0043231 intracellular membrane-bounded organelle
Orthologs
Species
Homo sapiens
Mus musculus
Gene ID
Gene Order
Pathway Predictions based on Human Orthology Data
NETPATH
REACTOME
Processive synthesis on the C-strand of the telomere pathway
Telomere C-strand (Lagging Strand) Synthesis pathway
Processive synthesis on the lagging strand pathway
Gap-filling DNA repair synthesis and ligation in TC-NER pathway
Transcription-coupled NER (TC-NER) pathway
Gap-filling DNA repair synthesis and ligation in GG-NER pathway
Resolution of D-loop structures through Holliday junction intermediates pathway
Removal of DNA patch containing abasic residue pathway
Resolution of AP sites via the multiple-nucleotide patch replacement pathway pathway
DNA Replication pathway
Synthesis of DNA pathway
Homologous Recombination Repair pathway
Resolution of Abasic Sites (AP sites) pathway
S Phase pathway
Chromosome Maintenance pathway
Global Genomic NER (GG-NER) pathway
Telomere Maintenance pathway
Double-Strand Break Repair pathway
Cell Cycle pathway
Mismatch repair (MMR) directed by MSH2:MSH6 (MutSalpha) pathway
Resolution of D-loop structures pathway
Base Excision Repair pathway
Homologous recombination repair of replication-independent double-strand breaks pathway
Cell Cycle, Mitotic pathway
DNA strand elongation pathway
Mismatch repair (MMR) directed by MSH2:MSH3 (MutSbeta) pathway
Mismatch Repair pathway
Extension of Telomeres pathway
Lagging Strand Synthesis pathway
Nucleotide Excision Repair pathway
DNA Repair pathway
KEGG
DNA replication pathway
Nucleotide excision repair pathway
Mismatch repair pathway
Base excision repair pathway
DNA replication pathway
Nucleotide excision repair pathway
Base excision repair pathway
Mismatch repair pathway
INOH
PID NCI
Cross-References
SwissProt
TrEMBL A4IFC8
UniProt Splice Variant
Entrez Gene 100124507
UniGene Bt.12876
RefSeq NM_001102548 XM_005219129 XM_005219130 XM_005219131
HUGO
OMIM
CCDS
HPRD
IMGT
EMBL BC134518 DAAA02047435
GenPept AAI34519
RNA Seq Atlas 100124507