DNTTIP1
Deoxynucleotidyltransferase terminal-interacting protein 1
Also known as: C20orf167, dJ447F3.4, Tdif1, TDIF1_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q9H147
- Gene
- DNTTIP1
- Ensembl
- ENSG00000101457
- Chromosome
- 20
- Canonical length
- 329 aa
- Protein class
- Plasma proteins, Predicted intracellular proteins
- Subcellular location
- Nucleoplasm,Nucleoli,Nucleoli rim,Mitotic chromosome
- Quaternary structure
- Homotrimer
OverviewNCBI Gene
DNTTIP1 binds DNA and enhances the activity of terminal deoxynucleotidyltransferase (TDT, or DNTT; MIM 187410), a DNA polymerase that catalyzes the polymerization of DNA in the absence of a DNA template (Yamashita et al., 2001 [PubMed 11473582]).[supplied by OMIM, Mar 2008]
Canonical amino-acid sequenceUniProt
329 residues, UniProt reviewed canonical sequence.
>Q9H147|DNTTIP1
1 MGATGDAEQP RGPSGAERGG LELGDAGAAG QLVLTNPWNI MIKHRQVQRR GRRSQMTTSF
61 TDPAISMDLL RAVLQPSINE EIQTVFNKYM KFFQKAALNV RDNVGEEVDA EQLIQEACRS
121 CLEQAKLLFS DGEKVIPRLT HELPGIKRGR QAEEECAHRG SPLPKKRKGR PPGHILSSDR
181 AAAGMVWKPK SCEPIRREGP KWDPARLNES TTFVLGSRAN KALGMGGTRG RIYIKHPHLF
241 KYAADPQDKH WLAEQHHMRA TGGKMAYLLI EEDIRDLAAS DDYRGCLDLK LEELKSFVLP
301 SWMVEKMRKY METLRTENEH RAVEAPPQTLocalizationUniProt · AlphaFold · HPA
Whether an antibody against DNTTIP1 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)
- 0.5
- Highest tissue expression
- 62 nTPM
Expression across tissuesHPA
Tissue
- skeletal muscle: 62 nTPM
- bone marrow: 42 nTPM
- urinary bladder: 37 nTPM
- rectum: 36 nTPM
- choroid plexus: 33 nTPM
- colon: 33 nTPM
Single-cell type
- neutrophils: 161 nCPM
- goblet cells: 103 nCPM
- megakaryocytes: 93 nCPM
- late primary spermatocytes: 91 nCPM
- hofbauer cells: 87 nCPM
- cytotrophoblasts: 78 nCPM
Immune cell
- neutrophil: 126 nTPM
- eosinophil: 71 nTPM
- classical monocyte: 51 nTPM
- myeloid DC: 43 nTPM
- intermediate monocyte: 22 nTPM
- basophil: 17 nTPM
Brain region
- midbrain: 22 nTPM
- white matter: 22 nTPM
- hypothalamus: 22 nTPM
- choroid plexus: 21 nTPM
- spinal cord: 20 nTPM
- cerebral cortex: 20 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)
- 0.42
- gnomAD pLI
- 0.73
- gnomAD missense Z
- 2.12
- DepMap mean gene effect
- -0.06
- DepMap dependency class
- selective
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 10% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
- Terminal deoxynucleotidyltransferase-interacting factor 1
- DNTTIP1, dimerisation domain
- TdIF1, C-terminal
- DNTTIP1 dimerisation domain
- TdIF1, C-terminal
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of DNTTIP1 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 DNTTIP1 as an antibody target. Whether an autoantibody or antibody against DNTTIP1 could matter depends on whether native DNTTIP1 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
DNTTIP1 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 DNTTIP1 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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