HUS1B
Checkpoint protein HUS1B
Also known as: HUS1B_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q8NHY5
- Gene
- HUS1B
- Ensembl
- ENSG00000188996
- Chromosome
- 6
- Canonical length
- 278 aa
- Protein class
- Predicted intracellular proteins
- Subcellular location
- Nucleoplasm,Cytosol
OverviewNCBI Gene
The protein encoded by this gene is most closely related to HUS1, a component of a cell cycle checkpoint protein complex involved in cell cycle arrest in response to DNA damage. This protein can interact with the check point protein RAD1 but not with RAD9. Overexpression of this protein has been shown to induce cell death, which suggests a related but distinct role of this protein, as compared to the HUS1. [provided by RefSeq, Jul 2008]
Canonical amino-acid sequenceUniProt
278 residues, UniProt reviewed canonical sequence.
>Q8NHY5|HUS1B
1 MKFRAKITGK GCLELFIHVS GTVARLAKVC VLRVRPDSLC FGPAGSGGLH EARLWCEVRQ
61 GAFQQFRMEG VSEDLDEIHL ELTAEHLSRA ARSAAGASSL KLQLTHKRRP SLTVAVELVS
121 SLGRARSVVH DLPVRVLPRR VWRDCLPPSL RASDASIRLP RWRTLRSIVE RMANVGSHVL
181 VEANLSGRMT LSIETEVVSI QSYFKNLGNP PQSAVGVPEN RDLESMVQVR VDNRKLLQFL
241 EGQQIHPTTA LCNIWDNTLL QLVLVQEDVS LQYFIPALLocalizationUniProt · AlphaFold · HPA
Whether an antibody against HUS1B 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)
- 0.27
- Highest tissue expression
- 2 nTPM
Expression across tissuesHPA
Tissue
- testis: 2 nTPM
- prostate: 0.7 nTPM
- bone marrow: 0.6 nTPM
- cervix: 0.6 nTPM
- lung: 0.6 nTPM
- skin: 0.6 nTPM
Single-cell type
- adipocytes: 0 nCPM
- adrenal cortex cells: 0 nCPM
- adrenal medulla cells: 0 nCPM
- alveolar cells type 1: 0 nCPM
- alveolar cells type 2: 0 nCPM
- astrocytes: 0 nCPM
Immune cell
- naive CD8 T-cell: 0.3 nTPM
- memory B-cell: 0.2 nTPM
- plasmacytoid DC: 0.2 nTPM
- classical monocyte: 0.1 nTPM
- gdT-cell: 0.1 nTPM
- memory CD4 T-cell: 0.1 nTPM
Brain region
- choroid plexus: 2.4 nTPM
- white matter: 2.4 nTPM
- cerebral cortex: 2.3 nTPM
- medulla oblongata: 2.3 nTPM
- amygdala: 2.2 nTPM
- pons: 2.2 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 missense Z
- -0.45
- DepMap mean gene effect
- 0.08
- DepMap dependency class
- none
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 5% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
- double-strand break repair via homologous recombination
- meiotic DNA integrity checkpoint signaling
- mitotic DNA replication checkpoint signaling
- mitotic intra-S DNA damage checkpoint signaling
- nucleotide-excision repair
- telomere maintenance
Cellular components
Protein domainsUniProt · Pfam · InterPro
InteractionsUniProt · HPA
Protein binding partners of HUS1B 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 HUS1B as an antibody target. Whether an autoantibody or antibody against HUS1B could matter depends on whether native HUS1B is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
HUS1B 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 HUS1B as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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