1. Gene
  2. POLD3 - DNA polymerase delta 3, accessory subunit Gene

POLD3 - DNA polymerase delta 3, accessory subunit Gene

Homo sapiens

Also known as P66; P68; PPP1R128

Gene ID: 10714 | Gene type: protein coding

About POLD3

Cytogenetic location: 11q13.4 Genomic coordinates (GRCh38): 11:74,592,582-74,669,341 (from NCBI)

This gene has 10 transcripts (splice variants) and 37 orthologues. Ubiquitous expression in testis (RPKM 7.5), colon (RPKM 6.2) and 25 other tissues.

Summary

This gene encodes the 66-kDa subunit of DNA Polymerase delta. DNA Polymerase delta possesses both polymerase and 3' to 5' exonuclease activity and plays a critical role in DNA replication and repair. The encoded protein plays a role in regulating the activity of DNA Polymerase delta through interactions with Other subunits and the processivity cofactor proliferating cell nuclear antigen (PCNA). Alternatively spliced transcript variants have been observed for this gene. [provided by RefSeq, Mar 2012]

POLD3 Products(2)

mRNA Protein Name
NM_001363597.2 NP_001350526.1 DNA polymerase delta subunit 3 isoform 2
NM_006591.3 NP_006582.1 DNA polymerase delta subunit 3 isoform 1
Gene Ontology
  • Molecular Function
  • Biological Process
  • Cellular Component
Molecular Function GO Annotation Evidence Reference Source
enables protein binding IPI
IPI: Inferred from physical interaction
15576034 GOA
enables protein-macromolecule adaptor activity IPI
IPI: Inferred from physical interaction
11595739 GOA
Biological Process GO Annotation Evidence Reference Source
involved in DNA biosynthetic process IDA
IDA: Inferred from direct assay
11595739 GOA
involved in DNA-templated DNA replication IDA
IDA: Inferred from direct assay
20334433 GOA
involved in error-prone translesion synthesis IDA
IDA: Inferred from direct assay
24449906 GOA
involved in nucleotide-excision repair, DNA gap filling IMP
IMP: Inferred from mutant phenotype
20227374 GOA
Cellular Component GO Annotation Evidence Reference Source
part of delta DNA polymerase complex IDA
IDA: Inferred from direct assay
11595739 GOA
part of delta DNA polymerase complex IPI
IPI: Inferred from physical interaction
12403614 GOA
part of zeta DNA polymerase complex IDA
IDA: Inferred from direct assay
22465957 GOA
part of zeta DNA polymerase complex IPI
IPI: Inferred from physical interaction
24449906 GOA
EXP: Inferred from Experiment IDA: Inferred from direct assay IPI: Inferred from physical interaction IMP: Inferred from mutant phenotype IGI: Inferred from genetic interaction IEP: Inferred from expression pattern

POLD3 Protein Structure

CDC27

CDC27: DNA polymerase subunit Cdc27 (19 - 466)

  • 0
  • 100
  • 200
  • 300
  • 400
  • 466 a.a.
Protein Preferred Names Protein Names

DNA polymerase delta subunit 3

DNA polymerase delta subunit C

POLD3 Protein-protein interaction Information

Type
Protein Name Protein ID Interactor Interactor Species Interactor ID Detection Method Reference
Intra
POLD3 Q15054 PCNA Homo sapiens P12004 16000169
Intra
POLD3 Q15054 POLD2 Homo sapiens P49005 16000169
Intra
POLD3 Q15054 POLD2 Homo sapiens P49005
Y2H
16000169
Cross: Cross-species interaction Intra: Intraspecies interaction

Related Diseases

Diseases Alias
Ruijs-Aalfs Syndrome

Progeroid Features-Hepatocellular Carcinoma Predisposition Syndrome

RJALS

Xeroderma Pigmentosum, Variant Type

Xeroderma Pigmentosum

XPV

Xeroderma Pigmentosum Variant Type

Xeroderma Pigmentosum With Normal Dna Repair Rates

Photosensitivity With Defective Dna Synthesis

Xp

De Sanctis-Cacchione Syndrome

Desanctis-Cacchione Syndrome

Xeroderma Pigmentosa

Xerodermic Idiocy

Xeroderma Pigmentosum Variant

Xp - [Xeroderma Pigmentosum]

Atrophoderma Pigmentosum

Chronic Fatigue Syndrome

Myalgic Encephalomyelitis

Postviral Fatigue Syndrome

Cfs

Myalgic Encephalitis

Encephalomyelitis, Myalgic

Chronic Fatigue

Fatigue Syndrome, Chronic

Benign Myalgic Encephalomyelitis

Akureyri

Akureyri Disease

Cfs - [Chronic Fatigue Syndrome]

Epidemic Neuromyasthenia

Myalgic Encephalomyelitis Syndrome

Me - [Myalgic Encephalomyelitis]

Pvfs - [Postviral Fatigue Syndrome]

Neuromyasthenia

Iceland Disease

Icelandic Disease

Fanconi Anemia, Complementation Group A

Fanconi Anemia

Fanconi Pancytopenia

Fanconi Anemia Complementation Group A

FANCA

Fa

Fanconi Panmyelopathy

Fanconi'S Anemia

Fanconi Anaemia

Fanconi'S Anaemia

Fanconi Hypoplastic Anemia

Estren-Dameshek Variant Of Fanconi Anemia

Estren-Dameshek Variant Of Fanconi Pancytopenia

Fanconi Anemia Estren-Dameshek Variant

Fanconis Anemia

Diseases Alias
Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Orthologs Information

Species Symbol Source ID
Bos taurus POLD3 VGNC VGNC:33115
Macaca mulatta POLD3 VGNC VGNC:101381
Mus musculus POLD3 MGD MGI:1915217
Felis catus POLD3 VGNC VGNC:64283
Rattus norvegicus POLD3 RGD RGD:1312027
Canis familiaris POLD3 VGNC VGNC:44776