Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
3980
Gene name Gene Name - the full gene name approved by the HGNC.
DNA ligase 3
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
LIG3
Synonyms (NCBI Gene) Gene synonyms aliases
LIG2, LIG3alpha, MTDPS20
Disease Acronyms (UniProt) Disease acronyms from UniProt database
MTDPS20
Chromosome Chromosome number
17
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
17q12
Summary Summary of gene provided in NCBI Entrez Gene.
This gene is a member of the DNA ligase family. Each member of this family encodes a protein that catalyzes the joining of DNA ends but they each have a distinct role in DNA metabolism. The protein encoded by this gene is involved in excision repair and i
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT028636 hsa-miR-30a-5p Proteomics 18668040
MIRT045688 hsa-miR-149-5p CLASH 23622248
MIRT1109235 hsa-miR-199a-3p CLIP-seq
MIRT1109236 hsa-miR-199b-3p CLIP-seq
MIRT1109237 hsa-miR-3129-5p CLIP-seq
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0000724 Process Double-strand break repair via homologous recombination TAS
GO:0003677 Function DNA binding IEA
GO:0003909 Function DNA ligase activity IDA 9809069
GO:0003909 Function DNA ligase activity TAS
GO:0003910 Function DNA ligase (ATP) activity IBA 21873635
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
600940 6600 ENSG00000005156
Protein
UniProt ID P49916
Protein name DNA ligase 3 (EC 6.5.1.1) (DNA ligase III) (Polydeoxyribonucleotide synthase [ATP] 3)
Protein function Isoform 3 functions as a heterodimer with DNA-repair protein XRCC1 in the nucleus and can correct defective DNA strand-break repair and sister chromatid exchange following treatment with ionizing radiation and alkylating agents. Isoform 1 is tar
PDB 1IMO , 1IN1 , 1UW0 , 3L2P , 3PC7 , 3PC8 , 3QVG , 6WH1
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00645 zf-PARP 96 181 Poly(ADP-ribose) polymerase and DNA-Ligase Zn-finger region Domain
PF04675 DNA_ligase_A_N 263 434 DNA ligase N terminus Family
PF01068 DNA_ligase_A_M 483 677 ATP dependent DNA ligase domain Domain
PF04679 DNA_ligase_A_C 704 814 Family
PF16759 LIG3_BRCT 933 1005 DNA ligase 3 BRCT domain Family
Tissue specificity TISSUE SPECIFICITY: Testis, thymus, prostate and heart.
Sequence
MSLAFKIFFPQTLRALSRKELCLFRKHHWRDVRQFSQWSETDLLHGHPLFLRRKPVLSFQ
GSHLRSRATYLVFLPGLHVGLCSGPCEMAEQRFCVDYAKRGTAGCKKCKEKIVKGVCRIG
KVVPNPFSESGGDMKEWYHIKCMFEKLERARATTKKIEDLTELEGWEELEDNEKEQITQH
I
ADLSSKAAGTPKKKAVVQAKLTTTGQVTSPVKGASFVTSTNPRKFSGFSAKPNNSGEAP
SSPTPKRSLSSSKCDPRHKDCLLREFRKLCAMVADNPSYNTKTQIIQDFLRKGSAGDGFH
GDVYLTVKLLLPGVIKTVYNLNDKQIVKLFSRIFNCNPDDMARDLEQGDVSETIRVFFEQ
SKSFPPAAKSLLTIQEVDEFLLRLSKLTKEDEQQQALQDIASRCTANDLKCIIRLIKHDL
KMNSGAKHVLDALD
PNAYEAFKASRNLQDVVERVLHNAQEVEKEPGQRRALSVQASLMTP
VQPMLAEACKSVEYAMKKCPNGMFSEIKYDGERVQVHKNGDHFSYFSRSLKPVLPHKVAH
FKDYIPQAFPGGHSMILDSEVLLIDNKTGKPLPFGTLGVHKKAAFQDANVCLFVFDCIYF
NDVSLMDRPLCERRKFLHDNMVEIPNRIMFSEMKRVTKALDLADMITRVIQEGLEGLVLK
DVKGTYEPGKRHWLKVK
KDYLNEGAMADTADLVVLGAFYGQGSKGGMMSIFLMGCYDPGS
QKWCTVTKCAGGHDDATLARLQNELDMVKISKDPSKIPSWLKVNKIYYPDFIVPDPKKAA
VWEITGAEFSKSEAHTADGISIRFPRCTRIRDDK
DWKSATNLPQLKELYQLSKEKADFTV
VAGDEGSSTTGGSSEENKGPSGSAVSRKAPSKPSASTKKAEGKLSNSNSKDGNMQTAKPS
AMKVGEKLATKSSPVKVGEKRKAADETLCQTKVLLDIFTGVRLYLPPSTPDFSRLRRYFV
AFDGDLVQEFDMTSATHVLGSRDKNPAAQQVSPEWIWACIRKRRL
VAPC
Sequence length 1009
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  KEGG   Reactome
  Base excision repair   Resolution of AP sites via the single-nucleotide replacement pathway
APEX1-Independent Resolution of AP Sites via the Single Nucleotide Replacement Pathway
HDR through MMEJ (alt-NHEJ)
Gap-filling DNA repair synthesis and ligation in GG-NER
Gap-filling DNA repair synthesis and ligation in TC-NER
Associated diseases Disease information provided by ClinVar, GenCC, and GWAS databases.
Causal
Disease term Disease name dbSNP ID References
Colorectal cancer Colorectal Carcinoma rs137854568, rs137854573, rs137854575, rs387906234, rs121908380, rs121908702, rs267606674, rs794729661, rs121909055, rs281865417, rs267606884, rs28934575, rs587776769, rs104893815, rs587776800
View all (467 more)
Unknown
Disease term Disease name Evidence References Source
Mitochondrial DNA Deletion Syndrome mitochondrial DNA depletion syndrome 20 (mngie type) GenCC
Restless Legs Syndrome Restless Legs Syndrome GWAS
Associations from Text Mining
Disease Name Relationship Type References
Adenoma Associate 23951112
Alzheimer Disease Associate 29474873
Anencephaly Associate 30022792
Bloom Syndrome Associate 8265359
Breast Neoplasms Associate 40493574
Carcinoma Hepatocellular Associate 30310528
Carcinoma Squamous Cell Associate 28334093
Colorectal Neoplasms Associate 26649135, 32312920
Diabetes Mellitus Associate 19147782
Drug Related Side Effects and Adverse Reactions Associate 36988399