Summary | |
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Symbol | H1F0 |
Name | H1 histone family, member 0 |
Aliases | H10; H1.0, H1(0), H1-0; H1FV; histone H1'; histone H1(0); Histone H1.0 |
Chromosomal Location | 22q13.1 |
External Links | HGNC, NCBI, Ensembl, Uniprot, GeneCards |
Content |
Basic function annotation. > Subcellular Location, Domain and Function > Gene Ontology > KEGG and Reactome Pathway |
Subcellular Location | Nucleus Chromosome Note=The RNA edited version has been localized to nuclear speckles. During mitosis, it appears in the vicinity of condensed chromosomes. |
Domain |
PF00538 linker histone H1 and H5 family |
Function |
Histones H1 are necessary for the condensation of nucleosome chains into higher-order structures. The H1F0 histones are found in cells that are in terminal stages of differentiation or that have low rates of cell division. |
Biological Process |
GO:0000737 DNA catabolic process, endonucleolytic GO:0006308 DNA catabolic process GO:0006309 apoptotic DNA fragmentation GO:0006323 DNA packaging GO:0006333 chromatin assembly or disassembly GO:0006334 nucleosome assembly GO:0006921 cellular component disassembly involved in execution phase of apoptosis GO:0019439 aromatic compound catabolic process GO:0030262 apoptotic nuclear changes GO:0031497 chromatin assembly GO:0034655 nucleobase-containing compound catabolic process GO:0034728 nucleosome organization GO:0044270 cellular nitrogen compound catabolic process GO:0046700 heterocycle catabolic process GO:0065004 protein-DNA complex assembly GO:0071103 DNA conformation change GO:0071824 protein-DNA complex subunit organization GO:0090305 nucleic acid phosphodiester bond hydrolysis GO:0097194 execution phase of apoptosis GO:1901361 organic cyclic compound catabolic process |
Molecular Function |
GO:0003682 chromatin binding GO:0031490 chromatin DNA binding GO:0043566 structure-specific DNA binding |
Cellular Component |
GO:0000785 chromatin GO:0000786 nucleosome GO:0000790 nuclear chromatin GO:0000791 euchromatin GO:0005719 nuclear euchromatin GO:0015629 actin cytoskeleton GO:0032993 protein-DNA complex GO:0044454 nuclear chromosome part GO:0044815 DNA packaging complex |
KEGG | - |
Reactome |
R-HSA-211227: Activation of DNA fragmentation factor R-HSA-109581: Apoptosis R-HSA-140342: Apoptosis induced DNA fragmentation R-HSA-75153: Apoptotic execution phase R-HSA-2559583: Cellular Senescence R-HSA-2262752: Cellular responses to stress R-HSA-2559586: DNA Damage/Telomere Stress Induced Senescence R-HSA-2559584: Formation of Senescence-Associated Heterochromatin Foci (SAHF) R-HSA-5357801: Programmed Cell Death |
Summary | |
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Symbol | H1F0 |
Name | H1 histone family, member 0 |
Aliases | H10; H1.0, H1(0), H1-0; H1FV; histone H1'; histone H1(0); Histone H1.0 |
Chromosomal Location | 22q13.1 |
External Links | HGNC, NCBI, Ensembl, Uniprot, GeneCards |
Content | Literatures that report relations between H1F0 and anti-tumor immunity. The specific mechanism were also collected if the literature reports that a gene specifically promotes or inhibits the infiltration or function of T/NK cells. |
There is no record. |
Summary | |
---|---|
Symbol | H1F0 |
Name | H1 histone family, member 0 |
Aliases | H10; H1.0, H1(0), H1-0; H1FV; histone H1'; histone H1(0); Histone H1.0 |
Chromosomal Location | 22q13.1 |
External Links | HGNC, NCBI, Ensembl, Uniprot, GeneCards |
Content | High-throughput screening data (e.g. CRISPR-Cas9, shRNA and RNAi) for T cell-mediated killing. Genetic screen techniques can identify mechanisms of tumor cell resistance (e.g., PTPN2) and sensitivity (e.g., APLNR) to killing by cytotoxic T cells, the central effectors of anti-tumor immunity. After comprehensively searching, eight groups of screening data sets were collected in the current database. In this tab, users can check whether their selected genes cause resistance or increase sensitivity to T cell-mediated killing in various data sets. |
> High-throughput Screening
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Statistical results of H1F0 in screening data sets for detecting immune reponses.
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Summary | |
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Symbol | H1F0 |
Name | H1 histone family, member 0 |
Aliases | H10; H1.0, H1(0), H1-0; H1FV; histone H1'; histone H1(0); Histone H1.0 |
Chromosomal Location | 22q13.1 |
External Links | HGNC, NCBI, Ensembl, Uniprot, GeneCards |
Content |
Transcriptomic and genomic profiling of pre-treated tumor biopsies from responders and non-responders to immunotherapy. These data were used to identify signatures and mechanisms of response to checkpoint blockade (e.g., anti-PDL1 and anti-PD1). One example is that mutations in the gene PBRM1 benefit clinical survival of patients with clear cell renal cell carcinoma. After comprehensively searching, we collected 5 and 6 of transcriptomic and genomic data sets, respectively. In this tab, users can check whether their selected genes have significant difference of expression or mutation between responders and non-responders in various data sets. > Expression difference between responders and non-responders > Mutation difference between responders and non-responders |
Points in the above scatter plot represent the expression difference of H1F0 in various data sets.
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There is no record. |
Summary | |
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Symbol | H1F0 |
Name | H1 histone family, member 0 |
Aliases | H10; H1.0, H1(0), H1-0; H1FV; histone H1'; histone H1(0); Histone H1.0 |
Chromosomal Location | 22q13.1 |
External Links | HGNC, NCBI, Ensembl, Uniprot, GeneCards |
Content |
Relations between abundance of tumor-infiltrating lymphocytes (TILs) and expression, copy number, methylation, or mutation of H1F0. The immune-related signatures of 28 TIL types from Charoentong's study, which can be viewed in the download page. For each cancer type, the relative abundance of TILs were inferred by using gene set variation analysis (GSVA) based on gene expression profile. In this tab, users can examine which kinds of TILs might be regulated by the current gene. |
Summary | |
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Symbol | H1F0 |
Name | H1 histone family, member 0 |
Aliases | H10; H1.0, H1(0), H1-0; H1FV; histone H1'; histone H1(0); Histone H1.0 |
Chromosomal Location | 22q13.1 |
External Links | HGNC, NCBI, Ensembl, Uniprot, GeneCards |
Content |
Relations between three kinds of immunomodulators and expression, copy number, methylation, or mutation of H1F0. These immunomo-dulators were collected from Charoentong's study. In this tab, users can examine which immunomodulators might be regulated by H1F0. > Immunoinhibitor > Immunostimulator > MHC molecule |
Summary | |
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Symbol | H1F0 |
Name | H1 histone family, member 0 |
Aliases | H10; H1.0, H1(0), H1-0; H1FV; histone H1'; histone H1(0); Histone H1.0 |
Chromosomal Location | 22q13.1 |
External Links | HGNC, NCBI, Ensembl, Uniprot, GeneCards |
Content |
Relations between chemokines (or receptors) and expression, copy number, methylation, or mutation of H1F0. In this tab, users can examine which chemokines (or receptors) might be regulated by the current gene. > Chemokine > Receptor |
Summary | |
---|---|
Symbol | H1F0 |
Name | H1 histone family, member 0 |
Aliases | H10; H1.0, H1(0), H1-0; H1FV; histone H1'; histone H1(0); Histone H1.0 |
Chromosomal Location | 22q13.1 |
External Links | HGNC, NCBI, Ensembl, Uniprot, GeneCards |
Content |
Distribution of H1F0 expression across immune and molecular subtypes. > Immune subtype > Molecular subtype |
Summary | |
---|---|
Symbol | H1F0 |
Name | H1 histone family, member 0 |
Aliases | H10; H1.0, H1(0), H1-0; H1FV; histone H1'; histone H1(0); Histone H1.0 |
Chromosomal Location | 22q13.1 |
External Links | HGNC, NCBI, Ensembl, Uniprot, GeneCards |
Content |
Associations between H1F0 and clinical features. > Overall survival analysis > Cancer stage > Tumor grade |