H2AC7
H2A clustered histone 7, the group of H2A histones
Basic information
Region (hg38): 6:26198784-26199293
Previous symbols: [ "H2AFG", "HIST1H2AD" ]
Links
Phenotypes
GenCC
Source:
No genCC data.
ClinVar
This is a list of variants' phenotypes submitted to
Variants pathogenicity by type
Statistics on ClinVar variants can assist in determining whether a specific variant type in the H2AC7 gene is commonly pathogenic or not.
In the table, we include only reliable ClinVar variants with their consequences to MANE Select, Mane Plus Clinical transcripts, or transcripts with TSL equals 1. Click the count to view the source variants.
Warning: slight differences between displayed counts and the number of variants in ClinVar may occur, primarily due to (1) the application of a different transcript and/or consequence by our variant effect predictor or (2) differences in clinical significance: we classify Benign/Likely benign variants as Likely benign and Pathogenic/Likely pathogenic variants as Likely pathogenic.
| Variant type | Pathogenic | Likely pathogenic | VUS | Likely benign | Benign | Sum |
|---|---|---|---|---|---|---|
| synonymous | 0 | |||||
| missense | 17 | 17 | ||||
| nonsense | 0 | |||||
| start loss | 0 | |||||
| frameshift | 0 | |||||
| inframe indel | 0 | |||||
| splice donor/acceptor (+/-2bp) | 0 | |||||
| splice region | 0 | |||||
| non coding | 0 | |||||
| Total | 0 | 0 | 17 | 0 | 0 |
Variants in H2AC7
This is a list of pathogenic ClinVar variants found in the H2AC7 region.
You can filter this list by clicking the number of variants in the Variants pathogenicity by type table.
| Position | Type | Phenotype | Significance | ClinVar |
|---|---|---|---|---|
| 6-26198865-C-T | not specified | Uncertain significance (Jan 23, 2025) | ||
| 6-26198870-T-C | not specified | Uncertain significance (Sep 01, 2021) | ||
| 6-26198870-T-G | not specified | Uncertain significance (Dec 03, 2021) | ||
| 6-26198964-G-C | not specified | Uncertain significance (Sep 02, 2024) | ||
| 6-26198984-G-C | not specified | Uncertain significance (Jan 21, 2025) | ||
| 6-26199033-C-G | not specified | Uncertain significance (Nov 15, 2021) | ||
| 6-26199038-T-G | not specified | Uncertain significance (Jul 11, 2022) | ||
| 6-26199084-C-A | not specified | Uncertain significance (Feb 27, 2025) | ||
| 6-26199096-C-A | not specified | Uncertain significance (May 11, 2022) | ||
| 6-26199134-T-C | not specified | Uncertain significance (Oct 07, 2024) | ||
| 6-26199137-C-T | not specified | Uncertain significance (Apr 30, 2024) | ||
| 6-26199153-C-T | not specified | Uncertain significance (May 23, 2023) | ||
| 6-26199164-G-A | not specified | Uncertain significance (May 05, 2023) | ||
| 6-26199170-T-C | not specified | Uncertain significance (Jun 06, 2023) | ||
| 6-26199177-C-T | not specified | Uncertain significance (Jul 30, 2023) | ||
| 6-26199194-G-T | not specified | Uncertain significance (Jan 02, 2024) | ||
| 6-26199201-C-A | not specified | Uncertain significance (Jun 26, 2024) | ||
| 6-26199212-G-A | not specified | Uncertain significance (Jul 26, 2024) | ||
| 6-26199224-T-C | not specified | Uncertain significance (Apr 18, 2024) | ||
| 6-26199234-G-A | not specified | Uncertain significance (Oct 26, 2021) | ||
| 6-26199236-C-G | not specified | Uncertain significance (Feb 18, 2025) |
GnomAD
Source:
| Gene | Type | Bio Type | Transcript | Coding Exons | Length |
|---|---|---|---|---|---|
| H2AC7 | protein_coding | protein_coding | ENST00000341023 | 1 | 393 |
| pLI Probability LOF Intolerant | pRec Probability LOF Recessive | Individuals with no LOFs | Individuals with Homozygous LOFs | Individuals with Heterozygous LOFs | Defined | p |
|---|---|---|---|---|---|---|
| 0.0000135 | 0.129 | 0 | 0 | 0 | 0 | 0.00 |
| Z-Score | Observed | Expected | Observed/Expected | Mutation Rate | Total Possible in Transcript | |
|---|---|---|---|---|---|---|
| Missense | -2.02 | 129 | 78.5 | 1.64 | 0.00000346 | 801 |
| Missense in Polyphen | 36 | 28.97 | 1.2426 | 305 | ||
| Synonymous | -8.05 | 100 | 37.4 | 2.68 | 0.00000170 | 297 |
| Loss of Function | -1.23 | 6 | 3.51 | 1.71 | 1.57e-7 | 35 |
LoF frequencies by population
| Ethnicity | Sum of pLOFs | p |
|---|---|---|
| African & African-American | 0.00 | 0.00 |
| Ashkenazi Jewish | 0.00 | 0.00 |
| East Asian | 0.00 | 0.00 |
| Finnish | 0.00 | 0.00 |
| European (Non-Finnish) | 0.00 | 0.00 |
| Middle Eastern | 0.00 | 0.00 |
| South Asian | 0.00 | 0.00 |
| Other | 0.00 | 0.00 |
dbNSFP
Source:
- Function
- FUNCTION: Core component of nucleosome. Nucleosomes wrap and compact DNA into chromatin, limiting DNA accessibility to the cellular machineries which require DNA as a template. Histones thereby play a central role in transcription regulation, DNA repair, DNA replication and chromosomal stability. DNA accessibility is regulated via a complex set of post-translational modifications of histones, also called histone code, and nucleosome remodeling.;
- Pathway
- Systemic lupus erythematosus - Homo sapiens (human);Necroptosis - Homo sapiens (human);Alcoholism - Homo sapiens (human);B-WICH complex positively regulates rRNA expression;ERCC6 (CSB) and EHMT2 (G9a) positively regulate rRNA expression;Positive epigenetic regulation of rRNA expression;SIRT1 negatively regulates rRNA expression;NoRC negatively regulates rRNA expression;Negative epigenetic regulation of rRNA expression;Signaling by WNT;Signal Transduction;DNA methylation;Epigenetic regulation of gene expression;Gene expression (Transcription);Generic Transcription Pathway;Oxidative Stress Induced Senescence;Senescence-Associated Secretory Phenotype (SASP);Cellular Senescence;Cellular responses to stress;Post-translational protein modification;HDACs deacetylate histones;Metabolism of proteins;Reproduction;RNA Polymerase I Promoter Clearance;RNA Polymerase I Promoter Opening;RNA Polymerase II Transcription;RUNX1 regulates genes involved in megakaryocyte differentiation and platelet function;RMTs methylate histone arginines;Chromatin modifying enzymes;RNA Polymerase I Transcription;Amyloid fiber formation;RNA Polymerase I Chain Elongation;Meiotic recombination;Metalloprotease DUBs;Meiosis;Activated PKN1 stimulates transcription of AR (androgen receptor) regulated genes KLK2 and KLK3;RHO GTPases activate PKNs;HATs acetylate histones;Cellular responses to external stimuli;RHO GTPase Effectors;Signaling by Rho GTPases;UCH proteinases;Packaging Of Telomere Ends;Telomere Maintenance;Chromosome Maintenance;Ub-specific processing proteases;Condensation of Prophase Chromosomes;Deubiquitination;Signaling by Nuclear Receptors;Chromatin organization;Mitotic Prophase;M Phase;Estrogen-dependent gene expression;Transcriptional regulation by small RNAs;RUNX1 regulates transcription of genes involved in differentiation of HSCs;Cell Cycle;Cell Cycle, Mitotic;ESR-mediated signaling;Transcriptional regulation by RUNX1;Formation of the beta-catenin:TCF transactivating complex;TCF dependent signaling in response to WNT;Gene Silencing by RNA;PRC2 methylates histones and DNA
(Consensus)
Intolerance Scores
- loftool
- 0.723
- rvis_EVS
- -0.58
- rvis_percentile_EVS
- 18.44
Haploinsufficiency Scores
- pHI
- 0.369
- hipred
- N
- hipred_score
- 0.146
- ghis
- 0.394
Essentials
- essential_gene_CRISPR
- N
- essential_gene_CRISPR2
- N
- essential_gene_gene_trap
- N
- gene_indispensability_pred
- E
- gene_indispensability_score
- 1.00
Gene Damage Prediction
| All | Recessive | Dominant | |
|---|---|---|---|
| Mendelian | Medium | Medium | Medium |
| Primary Immunodeficiency | Medium | Medium | Medium |
| Cancer | Medium | Medium | Medium |
Mouse Genome Informatics
- Gene name
- Hist1h2ab
- Phenotype
Gene ontology
- Biological process
- chromatin organization;biological_process
- Cellular component
- nucleosome;nuclear chromatin;nucleus;extracellular exosome
- Molecular function
- molecular_function;DNA binding;protein heterodimerization activity