SHLD3
Shieldin complex subunit 3
Also known as: AC008560.1, CTC-534A2.2, FLJ26957, RINN1, SHLD3_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q6ZNX1
- Gene
- SHLD3
- Ensembl
- ENSG00000253251
- Chromosome
- 5
- Canonical length
- 250 aa
- Protein class
- Predicted intracellular proteins
- Subcellular location
- Nucleoplasm,Nucleoli
OverviewNCBI Gene
Involved in negative regulation of double-strand break repair via homologous recombination; positive regulation of double-strand break repair via nonhomologous end joining; and positive regulation of isotype switching. Located in nucleolus; nucleoplasm; and site of double-strand break. [provided by Alliance of Genome Resources, Jul 2025]
Canonical amino-acid sequenceUniProt
250 residues, UniProt reviewed canonical sequence.
>Q6ZNX1|SHLD3
1 MTTEVILHYR PCESDPTQLP KIAEKAIQDF PTRPLSRFIP WFPYDGSKLP LRPKRSPPVI
61 SEEAAEDVKQ YLTISEHDAK SHSYDCTVDL LEFQPSLKKQ HLTWSHTLKE QTNSGNLGKQ
121 SEKGKQHKRR SWSISLPSNN CTKNVSPLSK KLQDSLKALN LHSLYRARWT IEHTICNSQT
181 LEDIWTKLNQ IIRHNELPSC NATIQRHLGQ IWVFCDIMYC EYVGSLLKGR LALTGKINLF
241 VHKYGVIFSMLocalizationUniProt · AlphaFold · HPA
Whether an antibody against SHLD3 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)
- 0.47
- Highest tissue expression
- 17 nTPM
Expression across tissuesHPA
Tissue
- bone marrow: 17 nTPM
- lymph node: 4.5 nTPM
- prostate: 4.1 nTPM
- breast: 4 nTPM
- thymus: 3.6 nTPM
- retina: 3.4 nTPM
Single-cell type
- innate lymphoid cells: 0.3 nCPM
- enteric stem cells: 0.2 nCPM
- corticotrophs: 0.1 nCPM
- erythrocyte progenitors: 0.1 nCPM
- melanocytes: 0.1 nCPM
- nk-cells: 0.1 nCPM
Immune cell
- basophil: 16 nTPM
- eosinophil: 6.4 nTPM
- T-reg: 6.2 nTPM
- naive CD4 T-cell: 6.1 nTPM
- naive CD8 T-cell: 5.6 nTPM
- NK-cell: 5 nTPM
Brain region
- white matter: 6 nTPM
- cerebral cortex: 5.4 nTPM
- cerebellum: 5.3 nTPM
- basal ganglia: 4.6 nTPM
- medulla oblongata: 4.5 nTPM
- spinal cord: 4.5 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)
- 1.01
- gnomAD pLI
- 0.02
OntologyGO
Biological processes
- DNA repair
- negative regulation of double-strand break repair via homologous recombination
- positive regulation of double-strand break repair via nonhomologous end joining
- positive regulation of isotype switching
- somatic diversification of immunoglobulins involved in immune response
- telomere maintenance in response to DNA damage
Cellular components
Protein domainsUniProt · Pfam · InterPro
- Shieldin complex subunit 3
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of SHLD3 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 SHLD3 as an antibody target. Whether an autoantibody or antibody against SHLD3 could matter depends on whether native SHLD3 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
SHLD3 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 SHLD3 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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