POLDIP2
Polymerase delta-interacting protein 2
Also known as: DKFZP586F1524, PDIP2_HUMAN, PDIP38
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q9Y2S7
- Gene
- POLDIP2
- Ensembl
- ENSG00000004142
- Chromosome
- 17
- Canonical length
- 368 aa
- Protein class
- Predicted intracellular proteins
- Subcellular location
- Mitochondria
OverviewNCBI Gene
This gene encodes a protein that interacts with the DNA polymerase delta p50 subunit, as well as with proliferating cell nuclear antigen. The encoded protein maybe play a role in the ability of the replication fork to bypass DNA lesions. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Feb 2014]
Canonical amino-acid sequenceUniProt
368 residues, UniProt reviewed canonical sequence.
>Q9Y2S7|POLDIP2
1 MAACTARRAL AVGSRWWSRS LTGARWPRPL CAAAGAGAFS PASTTTTRRH LSSRNRPEGK
61 VLETVGVFEV PKQNGKYETG QLFLHSIFGY RGVVLFPWQA RLYDRDVASA APEKAENPAG
121 HGSKEVKGKT HTYYQVLIDA RDCPHISQRS QTEAVTFLAN HDDSRALYAI PGLDYVSHED
181 ILPYTSTDQV PIQHELFERF LLYDQTKAPP FVARETLRAW QEKNHPWLEL SDVHRETTEN
241 IRVTVIPFYM GMREAQNSHV YWWRYCIRLE NLDSDVVQLR ERHWRIFSLS GTLETVRGRG
301 VVGREPVLSK EQPAFQYSSH VSLQASSGHM WGTFRFERPD GSHFDVRIPP FSLESNKDEK
361 TPPSGLHWLocalizationUniProt · AlphaFold · HPA
Whether an antibody against POLDIP2 can act on the native protein depends on physical access: surface and secreted proteins are reachable by circulating antibodies, intracellular proteins usually are not.
- Antibody reachability
- Intracellular
- Secreted
- No
- Transmembrane segments
- 0
- Mean surface accessibility (rSASA)
- 0.35
- Highest tissue expression
- 256 nTPM
Expression across tissuesHPA
Tissue
- skeletal muscle: 256 nTPM
- tongue: 196 nTPM
- liver: 163 nTPM
- heart muscle: 118 nTPM
- adrenal gland: 109 nTPM
- kidney: 95 nTPM
Single-cell type
- late spermatids: 249 nCPM
- esophageal apical cells: 168 nCPM
- esophageal suprabasal cells: 167 nCPM
- hepatocytes: 157 nCPM
- esophageal basal cells: 134 nCPM
- extravillous trophoblasts: 126 nCPM
Immune cell
- myeloid DC: 60 nTPM
- total PBMC: 53 nTPM
- memory B-cell: 49 nTPM
- classical monocyte: 49 nTPM
- intermediate monocyte: 47 nTPM
- memory CD8 T-cell: 44 nTPM
Brain region
- thalamus: 63 nTPM
- hypothalamus: 62 nTPM
- midbrain: 60 nTPM
- cerebral cortex: 60 nTPM
- medulla oblongata: 57 nTPM
- choroid plexus: 57 nTPM
Genetic constraint and essentialitygnomAD · DepMap
Does the body need this protein intact? Low LOEUF or a strong DepMap dependency means loss or blockade of the protein is likely to be felt.
- gnomAD LOEUF (loss-of-function intolerance)
- 0.46
- gnomAD pLI
- 0.41
- gnomAD missense Z
- 1.94
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 8% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
- DNA repair
- error-free translesion synthesis
- mitochondrion organization
- mitotic spindle assembly
- negative regulation of macroautophagy
- positive regulation of focal adhesion assembly
- positive regulation of mitotic cell cycle
- positive regulation of mitotic cytokinesis
- vascular associated smooth muscle cell proliferation
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of POLDIP2 in the human serome: UniProt-annotated complex subunits plus reported interactors. Each links to its own Seroatlas record.
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads POLDIP2 as an antibody target. Whether an autoantibody or antibody against POLDIP2 could matter depends on whether native POLDIP2 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
POLDIP2 is annotated as predominantly intracellular. Intracellular proteins are common autoantibody markers, becoming visible to the immune system after cell injury or altered processing, but are usually markers of disease rather than direct drivers.
Annotation status
The present source text does not explicitly label POLDIP2 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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