DNASE2B
Deoxyribonuclease-2-beta
Also known as: DLAD, DNS2B_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q8WZ79
- Gene
- DNASE2B
- Ensembl
- ENSG00000137976
- Chromosome
- 1
- Canonical length
- 361 aa
- Protein class
- Enzymes, Predicted intracellular proteins
- Secretome location
- Intracellular and membrane
OverviewNCBI Gene
The protein encoded by this gene shares considerable sequence similarity to, and is structurally related to DNase II. The latter is a well characterized endonuclease that catalyzes DNA hydrolysis in the absence of divalent cations at acidic pH. Unlike DNase II which is ubiquitously expressed, expression of this gene product is restricted to the salivary gland and lungs. The gene has been localized to chromosome 1p22.3 adjacent (and in opposite orientation) to the uricase pseudogene. Two transcript variants encoding different isoforms have been described for this gene. [provided by RefSeq, Jul 2008]
Canonical amino-acid sequenceUniProt
361 residues, UniProt reviewed canonical sequence.
>Q8WZ79|DNASE2B
1 MKQKMMARLL RTSFALLFLG LFGVLGAATI SCRNEEGKAV DWFTFYKLPK RQNKESGETG
61 LEYLYLDSTT RSWRKSEQLM NDTKSVLGRT LQQLYEAYAS KSNNTAYLIY NDGVPKPVNY
121 SRKYGHTKGL LLWNRVQGFW LIHSIPQFPP IPEEGYDYPP TGRRNGQSGI CITFKYNQYE
181 AIDSQLLVCN PNVYSCSIPA TFHQELIHMP QLCTRASSSE IPGRLLTTLQ SAQGQKFLHF
241 AKSDSFLDDI FAAWMAQRLK THLLTETWQR KRQELPSNCS LPYHVYNIKA IKLSRHSYFS
301 SYQDHAKWCI SQKGTKNRWT CIGDLNRSPH QAFRSGGFIC TQNWQIYQAF QGLVLYYESC
361 KLocalizationUniProt · AlphaFold · HPA
Whether an antibody against DNASE2B 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)
- 0.26
- Highest tissue expression
- 160 nTPM
Expression across tissuesHPA
Tissue
- salivary gland: 160 nTPM
- prostate: 6.3 nTPM
- lung: 2.3 nTPM
- skeletal muscle: 1.5 nTPM
- basal ganglia: 1 nTPM
- spinal cord: 1 nTPM
Single-cell type
- salivary acinar cells: 98 nCPM
- salivary myoepithelial cells: 52 nCPM
- lacrimal acinar cells: 34 nCPM
- macrophages: 9.9 nCPM
- neutrophils: 6.5 nCPM
- prostatic glandular cells: 6.5 nCPM
Immune cell
- basophil: 0 nTPM
- classical monocyte: 0 nTPM
- eosinophil: 0 nTPM
- gdT-cell: 0 nTPM
- intermediate monocyte: 0 nTPM
- MAIT T-cell: 0 nTPM
Brain region
- hypothalamus: 1.7 nTPM
- white matter: 1.4 nTPM
- basal ganglia: 0.9 nTPM
- medulla oblongata: 0.9 nTPM
- cerebral cortex: 0.6 nTPM
- pons: 0.6 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)
- 1.63
- gnomAD pLI
- 0
- gnomAD missense Z
- 0.16
- DepMap mean gene effect
- -0.03
- DepMap dependency class
- selective
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 3% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads DNASE2B as an antibody target. Whether an autoantibody or antibody against DNASE2B could matter depends on whether native DNASE2B is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
DNASE2B 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 DNASE2B as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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