H3-5
Histone H3.3C
Also known as: H3.3C, H3.5, H3C_HUMAN, H3F3C
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q6NXT2
- Gene
- H3-5
- Ensembl
- ENSG00000188375
- Chromosome
- 12
- Canonical length
- 135 aa
- Protein class
- Predicted intracellular proteins
- Subcellular location
- Nucleoplasm,Acrosome,Principal piece
OverviewNCBI Gene
Histones are basic nuclear proteins that are responsible for the nucleosome structure of the chromosomal fiber in eukaryotes. Nucleosomes consist of approximately 146 bp of DNA wrapped around a histone octamer composed of pairs of each of the four core histones (H2A, H2B, H3, and H4). The chromatin fiber is further compacted through the interaction of a linker histone, H1, with the DNA between the nucleosomes to form higher order chromatin structures. This gene contains introns and its mRNA is polyadenylated, unlike most histone genes. The protein encoded by this gene is a replication-independent histone that is a member of the histone H3 family. [provided by RefSeq, Oct 2015]
Canonical amino-acid sequenceUniProt
135 residues, UniProt reviewed canonical sequence.
>Q6NXT2|H3-5
1 MARTKQTARK STGGKAPRKQ LATKAARKST PSTCGVKPHR YRPGTVALRE IRRYQKSTEL
61 LIRKLPFQRL VREIAQDFNT DLRFQSAAVG ALQEASEAYL VGLLEDTNLC AIHAKRVTIM
121 PKDIQLARRI RGERALocalizationUniProt · AlphaFold · HPA
Whether an antibody against H3-5 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)
- 0.54
- Highest tissue expression
- 20 nTPM
Expression across tissuesHPA
Tissue
- testis: 20 nTPM
- bone marrow: 2.9 nTPM
- spleen: 1.3 nTPM
- appendix: 1 nTPM
- skin: 0.9 nTPM
- ovary: 0.8 nTPM
Single-cell type
- late primary spermatocytes: 231 nCPM
- early spermatids: 100 nCPM
- late spermatids: 15 nCPM
- early primary spermatocytes: 13 nCPM
- esophageal apical cells: 3.4 nCPM
- gastric chief cells: 3.3 nCPM
Immune cell
- neutrophil: 73 nTPM
- eosinophil: 42 nTPM
- total PBMC: 41 nTPM
- basophil: 37 nTPM
- memory B-cell: 16 nTPM
- intermediate monocyte: 16 nTPM
Brain region
- cerebral cortex: 0.8 nTPM
- basal ganglia: 0.1 nTPM
- medulla oblongata: 0.1 nTPM
- pons: 0.1 nTPM
- spinal cord: 0.1 nTPM
- white matter: 0.1 nTPM
DiseaseUniProt · ClinVar · IEDB · PubMed
Four sources answering four different questions about H3-5.
Disease | ImmuneIEDB
Conditions an epitope on H3-5 was assayed in.
- rheumatoid arthritis B cell
- onchocerciasis B cell
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
- gnomAD pLI
- 0
- DepMap mean gene effect
- 0.02
- DepMap dependency class
- selective
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 4% 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 H3-5 as an antibody target. Whether an autoantibody or antibody against H3-5 could matter depends on whether native H3-5 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
H3-5 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 H3-5 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
Loading the interactive Seroatlas protein explorer...