H2AC8

gene
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Also known as H2A/aH2A.1

Summary

H2AC8 (H2A clustered histone 8, HGNC:4724) is a protein-coding gene on chromosome 6p22.2, encoding Histone H2A type 1-B/E (P04908). Core component of nucleosome. It is a selective cancer dependency (DepMap: 29.3% of cell lines).

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 is intronless and encodes a replication-dependent histone that is a member of the histone H2A family. Transcripts from this gene lack polyA tails; instead, they contain a palindromic termination element. This gene is found in the large histone gene cluster on chromosome 6p22-p21.3.

Source: NCBI Gene 3012 — RefSeq curated summary.

At a glance

  • GWAS associations: 16
  • Clinical variants (ClinVar): 10 total
  • Cancer dependency (DepMap): dependent in 29.3% of screened cell lines
  • MANE Select transcript: NM_021052

Identifiers

Gene identifiers

FieldValue
HGNC IDHGNC:4724
Approved symbolH2AC8
NameH2A clustered histone 8
Location6p22.2
Locus typegene with protein product
StatusApproved
AliasesH2A/a, H2A.1
Ensembl geneENSG00000277075
Ensembl biotypeprotein_coding
OMIM602786
Entrez3012

Gene structure

Transcript identifiers

Ensembl transcripts: 2 — 2 protein_coding

ENST00000303910, ENST00000850583

RefSeq mRNA: 1 — MANE Select: NM_021052 NM_021052

CCDS: CCDS4595

Canonical transcript exons

ENST00000303910 — 1 exons

ExonStartEnd
ENSE000039783412621692126217437

Expression profiles

Bgee: expression breadth ubiquitous, 181 present calls, max score 96.96.

FANTOM5 (CAGE): breadth ubiquitous, TPM avg 397.2778 / max 7341.0468, expressed in 1806 samples.

FANTOM5 promoters (2 alternative TSS)

Promoter IDTPM avgSamples expressed
66491347.86801804
6649249.40981711

Top tissues by expression

281 total, by Bgee expression score (0-100, higher = more expressed):

TissueAnatomy IDExpression scoreQuality
calcaneal tendonUBERON:000370196.96gold quality
adrenal tissueUBERON:001830396.29gold quality
male germ line stem cell (sensu Vertebrata) in testisCL:0000089 ∩ UBERON:000047392.19gold quality
monocyteCL:000057690.10gold quality
mononuclear cellCL:000084289.16gold quality
primordial germ cell in gonadCL:0000670 ∩ UBERON:000099188.19gold quality
leukocyteCL:000073887.97gold quality
lower esophagus mucosaUBERON:003583487.20gold quality
tendonUBERON:000004386.20gold quality
bone marrow cellCL:000209285.70gold quality
right uterine tubeUBERON:000130284.28gold quality
mucosa of transverse colonUBERON:000499182.35gold quality
prostate glandUBERON:000236782.00gold quality
amniotic fluidUBERON:000017380.62gold quality
colonic epitheliumUBERON:000039779.61gold quality
C1 segment of cervical spinal cordUBERON:000646978.59gold quality
corpus epididymisUBERON:000435978.07gold quality
bloodUBERON:000017876.45gold quality
skin of abdomenUBERON:000141676.40gold quality
bone marrowUBERON:000237175.59gold quality
granulocyteCL:000009475.58gold quality
vaginaUBERON:000099674.90gold quality
spinal cordUBERON:000224074.90gold quality
corpus callosumUBERON:000233674.53gold quality
esophagus mucosaUBERON:000246973.15gold quality
thymusUBERON:000237072.86silver quality
apex of heartUBERON:000209872.62gold quality
skin of legUBERON:000151172.57gold quality
olfactory segment of nasal mucosaUBERON:000538672.23gold quality
ventricular zoneUBERON:000305372.01gold quality

Single-cell (SCXA)

Detected in 1 experiment(s), a significant marker in 1.

ExperimentMarker?Max mean expression
E-ANND-3yes9.98

Regulation

Is transcription factor: no

Upstream regulators (CollecTRI, top): E2F1, RBL1

miRNA regulators (miRDB)

17 targeting H2AC8, top 30 by miRDB confidence (max_score; target_count = how many genes the miRNA targets in total — lower means more specific):

miRNAMax scoreAvg scoremiRNA target_count
HSA-MIR-9-5P100.0072.282361
HSA-MIR-511-3P99.9968.851467
HSA-MIR-383-3P99.8565.841359
HSA-MIR-6756-5P99.8267.972466
HSA-MIR-674599.7465.331321
HSA-MIR-6766-5P99.6867.702325
HSA-MIR-29B-2-5P99.6768.981726
HSA-MIR-6512-3P99.6566.071468
HSA-MIR-6720-5P99.6566.221459
HSA-MIR-363-5P99.4664.511015
HSA-MIR-127699.3668.181642
HSA-MIR-146A-3P99.1368.991881
HSA-MIR-76098.8166.651392
HSA-MIR-448398.0964.121642
HSA-MIR-805797.6466.54897
HSA-MIR-6822-3P96.6066.06680
HSA-MIR-129396.1664.69916

Functional genomics

DepMap (CRISPR cell-line fitness): dependent in 29.3% of screened cell lines.

Cross-species orthologs

22 orthologs

OrganismSymbolGene ID
mus_musculusH2ac7ENSMUSG00000071478
rattus_norvegicusHist1h2acENSRNOG00000090744
drosophila_melanogasterHis2A:CG31618FBGN0051618
drosophila_melanogasterHis2A:CG33808FBGN0053808
drosophila_melanogasterHis2A:CG33814FBGN0053814
drosophila_melanogasterHis2A:CG33817FBGN0053817
drosophila_melanogasterHis2A:CG33820FBGN0053820
drosophila_melanogasterHis2A:CG33823FBGN0053823
drosophila_melanogasterHis2A:CG33826FBGN0053826
drosophila_melanogasterHis2A:CG33829FBGN0053829
drosophila_melanogasterHis2A:CG33832FBGN0053832
drosophila_melanogasterHis2A:CG33835FBGN0053835
drosophila_melanogasterHis2A:CG33838FBGN0053838
drosophila_melanogasterHis2A:CG33841FBGN0053841
drosophila_melanogasterHis2A:CG33844FBGN0053844
drosophila_melanogasterHis2A:CG33847FBGN0053847
drosophila_melanogasterHis2A:CG33850FBGN0053850
drosophila_melanogasterHis2A:CG33853FBGN0053853
drosophila_melanogasterHis2A:CG33856FBGN0053856
drosophila_melanogasterHis2A:CG33859FBGN0053859
drosophila_melanogasterHis2A:CG33862FBGN0053862
drosophila_melanogasterHis2A:CG33865FBGN0053865

Paralogs (27): MACROH2A2 (ENSG00000099284), H2AZ2 (ENSG00000105968), MACROH2A1 (ENSG00000113648), H2AZ1 (ENSG00000164032), H2AC1 (ENSG00000164508), H2AC6 (ENSG00000180573), H2AC25 (ENSG00000181218), H2AC20 (ENSG00000184260), H2AC21 (ENSG00000184270), H2AX (ENSG00000188486), H2AC13 (ENSG00000196747), H2AC11 (ENSG00000196787), H2AC7 (ENSG00000196866), H2AL3 (ENSG00000229674), H2AJ (ENSG00000246705), H2AL1Q (ENSG00000249467), H2AB1 (ENSG00000274183), H2AC12 (ENSG00000274997), H2AC15 (ENSG00000275221), H2AC14 (ENSG00000276368), H2AC16 (ENSG00000276903), H2AB3 (ENSG00000277745), H2AB2 (ENSG00000277858), H2AC4 (ENSG00000278463), H2AC17 (ENSG00000278677), H2AC18 (ENSG00000288825), H2AC19 (ENSG00000288859)

Protein

Protein identifiers

Histone H2A type 1-B/EP04908 (reviewed: P04908)

Alternative names: Histone H2A.2, Histone H2A/a, Histone H2A/m

All UniProt accessions (2): P04908, Q08AJ9

UniProt curated annotations — full annotation on UniProt →

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.

Subunit / interactions. The nucleosome is a histone octamer containing two molecules each of H2A, H2B, H3 and H4 assembled in one H3-H4 heterotetramer and two H2A-H2B heterodimers. The octamer wraps approximately 147 bp of DNA.

Subcellular location. Nucleus. Chromosome.

Post-translational modifications. Deiminated on Arg-4 in granulocytes upon calcium entry. Monoubiquitination of Lys-120 (H2AK119Ub) by RING1, TRIM37 and RNF2/RING2 complex gives a specific tag for epigenetic transcriptional repression and participates in X chromosome inactivation of female mammals. It is involved in the initiation of both imprinted and random X inactivation. Ubiquitinated H2A is enriched in inactive X chromosome chromatin. Ubiquitination of H2A functions downstream of methylation of ‘Lys-27’ of histone H3 (H3K27me). H2AK119Ub by RNF2/RING2 can also be induced by ultraviolet and may be involved in DNA repair. Monoubiquitination of Lys-120 (H2AK119Ub) by TRIM37 may promote transformation of cells in a number of breast cancers. Following DNA double-strand breaks (DSBs), it is ubiquitinated through ‘Lys-63’ linkage of ubiquitin moieties by the E2 ligase UBE2N and the E3 ligases RNF8 and RNF168, leading to the recruitment of repair proteins to sites of DNA damage. Ubiquitination at Lys-14 and Lys-16 (H2AK13Ub and H2AK15Ub, respectively) in response to DNA damage is initiated by RNF168 that mediates monoubiquitination at these 2 sites, and ‘Lys-63’-linked ubiquitin are then conjugated to monoubiquitin; RNF8 is able to extend ‘Lys-63’-linked ubiquitin chains in vitro. Deubiquitinated by USP51 at Lys-14 and Lys-16 (H2AK13Ub and H2AK15Ub, respectively) after damaged DNA is repaired. H2AK119Ub and ionizing radiation-induced ‘Lys-63’-linked ubiquitination (H2AK13Ub and H2AK15Ub) are distinct events. Phosphorylation on Ser-2 (H2AS1ph) is enhanced during mitosis. Phosphorylation on Ser-2 by RPS6KA5/MSK1 directly represses transcription. Acetylation of H3 inhibits Ser-2 phosphorylation by RPS6KA5/MSK1. Phosphorylation at Thr-121 (H2AT120ph) by DCAF1 is present in the regulatory region of many tumor suppresor genes and down-regulates their transcription. Glutamine methylation at Gln-105 (H2AQ104me) by FBL is specifically dedicated to polymerase I. It is present at 35S ribosomal DNA locus and impairs binding of the FACT complex. Symmetric dimethylation on Arg-4 by the PRDM1/PRMT5 complex may play a crucial role in the germ-cell lineage. Crotonylation (Kcr) is specifically present in male germ cells and marks testis-specific genes in post-meiotic cells, including X-linked genes that escape sex chromosome inactivation in haploid cells. Crotonylation marks active promoters and enhancers and confers resistance to transcriptional repressors. It is also associated with post-meiotically activated genes on autosomes. Lactylated in macrophages by EP300/P300 by using lactoyl-CoA directly derived from endogenous or exogenous lactate, leading to stimulates gene transcription.

Similarity. Belongs to the histone H2A family.

RefSeq proteins (1): NP_066390* (*=MANE)

Domains & families (InterPro)

IDNameType
IPR002119Histone_H2AFamily
IPR007125H2A/H2B/H3Domain
IPR009072Histone-foldHomologous_superfamily
IPR032454Histone_H2A_CDomain
IPR032458Histone_H2A_CSConserved_site

Pfam: PF00125, PF16211

UniProt features (58 total): modified residue 36, helix 6, strand 4, cross-link 3, turn 3, initiator methionine 1, chain 1, region of interest 1, compositionally biased region 1, mutagenesis site 1, sequence conflict 1

Structure

Experimental structures (PDB)

356 structures, top 30 by resolution.

PDBMethodResolution (Å)
7VZ4ELECTRON MICROSCOPY1.89
6ACLX-RAY DIFFRACTION1.92
8I17X-RAY DIFFRACTION1.98
5B0ZX-RAY DIFFRACTION1.99
5Y0DX-RAY DIFFRACTION1.99
6IPUX-RAY DIFFRACTION1.99
8UQAX-RAY DIFFRACTION2.05
5Y0CX-RAY DIFFRACTION2.09
8Q3EX-RAY DIFFRACTION2.17
5X7XX-RAY DIFFRACTION2.18
5AV6X-RAY DIFFRACTION2.2
5AV8X-RAY DIFFRACTION2.2
5AV9X-RAY DIFFRACTION2.2
5B31X-RAY DIFFRACTION2.2
6KE9X-RAY DIFFRACTION2.22
6IQ4X-RAY DIFFRACTION2.25
6JXDX-RAY DIFFRACTION2.25
8KB5ELECTRON MICROSCOPY2.26
8UQ9X-RAY DIFFRACTION2.3
8Q3XX-RAY DIFFRACTION2.3
8UQ8X-RAY DIFFRACTION2.34
5B32X-RAY DIFFRACTION2.35
8JLBELECTRON MICROSCOPY2.36
8YBJELECTRON MICROSCOPY2.38
3AZGX-RAY DIFFRACTION2.4
5AV5X-RAY DIFFRACTION2.4
5AVBX-RAY DIFFRACTION2.4
5AVCX-RAY DIFFRACTION2.4
6JR1X-RAY DIFFRACTION2.4
8JLDELECTRON MICROSCOPY2.48

Predicted structure (AlphaFold)

ModelpLDDTFraction very-high
AF-P04908-F191.030.80

Antibody-complex structures (SAbDab): 86E0C, 6E0P, 7K5X, 7K5Y, 7K60, 7K61, 7K63, 8VFX

Functional residue map

Curated UniProt residues grouped by drug-discovery relevance — catalytic, ligand-binding, modification, and mutation-validated positions. Source: UniProtKB sequence features.

Post-translational modifications (39): 10, 10, 10, 10, 10, 14, 14, 16, 37, 37, 37, 37, 75, 76, 96, 96, 96, 96, 96, 105 …

Mutagenesis-validated functional residues (1):

PositionPhenotype
2blocks the inhibition of transcription by rps6ka5/msk1.

Function

Pathways and Gene Ontology

Reactome pathways

55 pathways

IDPathway
R-HSA-110328Recognition and association of DNA glycosylase with site containing an affected pyrimidine
R-HSA-110329Cleavage of the damaged pyrimidine
R-HSA-110330Recognition and association of DNA glycosylase with site containing an affected purine
R-HSA-110331Cleavage of the damaged purine
R-HSA-1221632Meiotic synapsis
R-HSA-171306Packaging Of Telomere Ends
R-HSA-1912408Pre-NOTCH Transcription and Translation
R-HSA-201722Formation of the beta-catenin:TCF transactivating complex
R-HSA-212300PRC2 methylates histones and DNA
R-HSA-2299718Condensation of Prophase Chromosomes
R-HSA-2559580Oxidative Stress Induced Senescence
R-HSA-2559582Senescence-Associated Secretory Phenotype (SASP)
R-HSA-2559586DNA Damage/Telomere Stress Induced Senescence
R-HSA-3214815HDACs deacetylate histones
R-HSA-3214847HATs acetylate histones
R-HSA-3214858RMTs methylate histone arginines
R-HSA-427359SIRT1 negatively regulates rRNA expression
R-HSA-427389ERCC6 (CSB) and EHMT2 (G9a) positively regulate rRNA expression
R-HSA-427413NoRC negatively regulates rRNA expression
R-HSA-5250924B-WICH complex positively regulates rRNA expression
R-HSA-5334118DNA methylation
R-HSA-5578749Transcriptional regulation by small RNAs
R-HSA-5617472Activation of anterior HOX genes in hindbrain development during early embryogenesis
R-HSA-5625886Activated PKN1 stimulates transcription of AR (androgen receptor) regulated genes KLK2 and KLK3
R-HSA-5689603UCH proteinases
R-HSA-5689880Ub-specific processing proteases
R-HSA-5689901Metalloprotease DUBs
R-HSA-606279Deposition of new CENPA-containing nucleosomes at the centromere
R-HSA-68616Assembly of the ORC complex at the origin of replication
R-HSA-73728RNA Polymerase I Promoter Opening

MSigDB gene sets: 258 (showing top): GSE45365_NK_CELL_VS_CD8A_DC_MCMV_INFECTION_UP, REACTOME_MEIOTIC_RECOMBINATION, REACTOME_DNA_REPLICATION, REACTOME_SIGNALING_BY_NOTCH, REACTOME_ADAPTIVE_IMMUNE_SYSTEM, BERTUCCI_MEDULLARY_VS_DUCTAL_BREAST_CANCER_DN, REACTOME_MEIOTIC_SYNAPSIS, GOZGIT_ESR1_TARGETS_DN, GRAESSMANN_APOPTOSIS_BY_DOXORUBICIN_DN, KONG_E2F3_TARGETS, REACTOME_ADHERENS_JUNCTIONS_INTERACTIONS, GOBP_NEGATIVE_REGULATION_OF_GENE_EXPRESSION_EPIGENETIC, GOBP_PROTEIN_LOCALIZATION_TO_CHROMOSOME_CENTROMERIC_REGION, SHETH_LIVER_CANCER_VS_TXNIP_LOSS_PAM2, LE_EGR2_TARGETS_UP

GO Biological Process (4): chromatin organization (GO:0006325), negative regulation of cell population proliferation (GO:0008285), heterochromatin formation (GO:0031507), protein localization to CENP-A containing chromatin (GO:0061644)

GO Molecular Function (4): DNA binding (GO:0003677), structural constituent of chromatin (GO:0030527), protein heterodimerization activity (GO:0046982), protein binding (GO:0005515)

GO Cellular Component (5): nucleosome (GO:0000786), nucleus (GO:0005634), CENP-A containing nucleosome (GO:0043505), extracellular exosome (GO:0070062), chromosome (GO:0005694)

Reactome top-level categories

Rollup of top-12 pathways:

CategoryPathways
Cellular Senescence3
Chromatin modifying enzymes3
Depyrimidination2
Depurination2
Negative epigenetic regulation of rRNA expression2
Positive epigenetic regulation of rRNA expression2
Meiosis1
Telomere Maintenance1
Pre-NOTCH Expression and Processing1
TCF dependent signaling in response to WNT1
Epigenetic regulation of gene expression1
Mitotic Prophase1

GO top-level categories

Rollup of top GO terms by namespace:

CategoryTerms
chromatin2
cellular component organization1
cell population proliferation1
regulation of cell population proliferation1
negative regulation of cellular process1
cellular component assembly1
heterochromatin boundary formation1
negative regulation of gene expression, epigenetic1
heterochromatin organization1
protein localization to chromatin1
protein localization to chromosome, centromeric region1
nucleic acid binding1
structural molecule activity1
protein dimerization activity1
binding1
protein-DNA complex1
intracellular membrane-bounded organelle1
nucleosome1
CENP-A containing chromatin1
extracellular vesicle1
intracellular membraneless organelle1

Protein interactions and networks

STRING

2092 interactions, top by confidence (×1000):

Protein AProtein BPartner UniProtScore
H2AC8H2BC21Q16778940
H2AC8H4C16P02304856
H2AC8H3C1P02295846
H2AC8H1-1Q02539743
H2AC8H2BC8P02278690
H2AC8H2BC5P58876689
H2AC8H2BC3P33778634
H2AC8H2BC12O60814606
H2AC8H1-5P16401599
H2AC8H2BC14Q99879591
H2AC8H3C14Q71DI3563
H2AC8H3-3AP06351561
H2AC8UBA1P22314462
H2AC8H2BC17P23527452
H2AC8H1-2P16403438

IntAct

215 interactions, top by confidence:

ABTypeScore
H2AC4H4C16psi-mi:“MI:0915”(physical association)0.900
H2AC4H2BC11psi-mi:“MI:0915”(physical association)0.850
H2AC4H2BC11psi-mi:“MI:0407”(direct interaction)0.850
CXXC1SETD1Apsi-mi:“MI:0914”(association)0.760
XPCCETN3psi-mi:“MI:0914”(association)0.730
H2AC4PPM1Gpsi-mi:“MI:0914”(association)0.670
H3-4H2AC4psi-mi:“MI:0915”(physical association)0.590
HP1BP3H2AC4psi-mi:“MI:0915”(physical association)0.560
H2AC4H2BC15psi-mi:“MI:0915”(physical association)0.560
H2AC4H3C13psi-mi:“MI:0915”(physical association)0.550
H2AC4H2BC12psi-mi:“MI:0915”(physical association)0.530
CBX6IGF2BP3psi-mi:“MI:0914”(association)0.530
CBX1KPNA3psi-mi:“MI:0914”(association)0.530
H1-6ZNF724psi-mi:“MI:0914”(association)0.530
HP1BP3IPO8psi-mi:“MI:0914”(association)0.530
UBE3AHERC2psi-mi:“MI:0914”(association)0.500
psi-mi:“MI:0915”(physical association)0.500

BioGRID (1018): HIST1H2AE (Affinity Capture-MS), HIST1H2AB (Biochemical Activity), HIST1H2AB (Reconstituted Complex), HIST1H2AB (Affinity Capture-Western), HIST1H2AB (Affinity Capture-Western), UBC (Affinity Capture-Western), HIST1H2AE (Affinity Capture-RNA), HIST1H2AE (Affinity Capture-RNA), HIST1H2AE (Affinity Capture-RNA), HIST1H2AB (Biochemical Activity), HIST1H2AB (Biochemical Activity), HIST1H2AB (Biochemical Activity), HIST1H2AB (Biochemical Activity), HIST1H2AB (Reconstituted Complex), HIST1H2AB (Affinity Capture-Western)

ESM2 similar proteins: A1A4R1, A9UMV8, C0HKE1, C0HKE2, C0HKE3, C0HKE4, C0HKE5, C0HKE6, C0HKE7, C0HKE8, C0HKE9, P02262, P02263, P02270, P04908, P06897, P0C0S8, P0C0S9, P0C169, P0C170, P0CC09, P13912, P19178, P20671, P21896, P27325, P35061, P35062, P70082, P84052, Q07135, Q16777, Q3ZBX9, Q4FZT6, Q4R3X5, Q64522, Q64523, Q64598, Q6FI13, Q6GSS7

Diamond homologs: A0A097I1R9, A0A097I2B5, A0A0D2UG83, A1A4R1, A1CJ10, A1D8G8, A3LXE7, A3LZZ0, A5DBG4, A5DJJ2, A5DWF1, A5DXC6, A9UMV8, C0HKE1, C0HKE2, C0HKE3, C0HKE4, C0HKE5, C0HKE6, C0HKE7, C0HKE8, C0HKE9, L7HZV6, O74268, P02262, P02263, P02264, P04908, P04909, P04910, P04911, P04912, P06897, P07793, P08844, P0C0S8, P0C0S9, P0C169, P0C170, P0C952

SIGNOR signaling

8 interactions.

AEffectBMechanism
KDM4C“down-regulates activity”H2AC4demethylation
H2AC4“form complex”“Nucleosome_H3.3 variant”binding
SLBP“up-regulates quantity by expression”H2AC4“translation regulation”
DZIP3“up-regulates activity”H2AC4monoubiquitination
H2AC4“form complex”“CENP-A nucleosome”binding
H2AC4“form complex”“Nucleosome_H3.1 variant”binding
H2AC4“form complex”“Nucleosome_H3.1t variant”binding

Enriched among interaction partners

Reactome pathways and GO biological processes over-represented among this gene’s 186 IntAct physical interaction partners (hypergeometric vs the genome-wide background, BH-FDR, gene-set size 15–500, ranked by fold). A functional readout of the neighbourhood — distinct from this gene’s own memberships above, and biased toward well-studied / hub proteins, so read it as themes rather than proof.

Reactome pathways:

PathwayPartnersFoldFDR
Formation of Senescence-Associated Heterochromatin Foci (SAHF)631.7×3e-07
Replacement of protamines by nucleosomes in the male pronucleus1123.6×2e-11
Packaging Of Telomere Ends1220.8×1e-11
Recognition and association of DNA glycosylase with site containing an affected purine1219.3×2e-11
Cleavage of the damaged purine1219.3×2e-11
RNA Polymerase I Promoter Opening1318.9×7e-12
ChAHP complex assembly1318.9×7e-12
Inhibition of DNA recombination at telomere1418.5×2e-12

GO biological processes:

GO termPartnersFoldFDR
negative regulation of DNA recombination534.9×1e-04
chromosome condensation526.2×3e-04
nucleosome assembly1815.7×8e-14
chromatin organization116.8×2e-04
chromatin remodeling125.4×5e-04

Disease & clinical

Clinical variants and AI predictions

ClinVar

10 variants total. Per-class counts are floors (≥ shown; pagination cap):

ClassificationCount (floor)
Pathogenic0
Likely pathogenic0
Uncertain significance10
Likely benign0
Benign0

Top pathogenic / likely-pathogenic (0)

SpliceAI

54 predictions. Top by Δscore:

VariantEffectΔscore
6:26217088:C:Tdonor_gain0.8000
6:26217018:C:Gdonor_gain0.7400
6:26217199:G:GTdonor_gain0.6200
6:26217254:C:Gdonor_gain0.6100
6:26217230:C:Gdonor_gain0.6000
6:26217251:GAGC:Gdonor_gain0.6000
6:26217091:C:Gdonor_gain0.5400
6:26217195:A:AGdonor_gain0.5200
6:26217258:A:Gdonor_gain0.5200
6:26217271:T:TAdonor_gain0.5200
6:26217087:GCAAC:Gdonor_gain0.4900
6:26217122:GT:Gdonor_gain0.4900
6:26217258:A:AGdonor_gain0.4800
6:26217012:C:Tdonor_gain0.4600
6:26217262:GCTTC:Gdonor_gain0.4500
6:26217339:A:Tdonor_gain0.4500
6:26217250:G:GTdonor_gain0.4200
6:26217361:C:Tdonor_gain0.4200
6:26217291:G:Tdonor_gain0.3800
6:26217170:C:Gdonor_gain0.3700
6:26216982:G:GTdonor_gain0.3500
6:26217273:GC:Gdonor_gain0.3500
6:26217358:GG:Gdonor_gain0.3300
6:26217359:GG:Gdonor_gain0.3300
6:26217290:G:GTdonor_gain0.3200
6:26217314:G:GTdonor_gain0.3200
6:26216989:A:Tdonor_gain0.3100
6:26217272:CG:Cdonor_gain0.3100
6:26217313:GGCC:Gdonor_gain0.3100
6:26217128:C:Gdonor_gain0.3000

AlphaMissense

818 scored. Top likely-pathogenic:

VariantProtein changeam_pathogenicity
6:26217146:T:CY58H1.000
6:26217171:T:CL66P1.000
6:26217176:G:CG68R1.000
6:26217177:G:AG68D1.000
6:26217186:C:AA71D1.000
6:26217231:T:CL86P1.000
6:26217245:G:CD91H1.000
6:26217246:A:CD91A1.000
6:26217246:A:TD91V1.000
6:26217045:T:AL24H0.999
6:26217045:T:CL24P0.999
6:26217051:T:CF26S0.999
6:26217057:T:AV28D0.999
6:26217059:G:CG29R0.999
6:26217060:G:AG29D0.999
6:26217107:G:TG45W0.999
6:26217108:G:AG45E0.999
6:26217134:G:CA54P0.999
6:26217135:C:AA54E0.999
6:26217143:G:AE57K0.999
6:26217144:A:TE57V0.999
6:26217150:T:CL59P0.999
6:26217155:G:CA61P0.999
6:26217156:C:AA61D0.999
6:26217158:G:AE62K0.999
6:26217159:A:TE62V0.999
6:26217167:G:AE65K0.999
6:26217173:G:CA67P0.999
6:26217174:C:AA67D0.999
6:26217176:G:TG68C0.999

dbSNP variants (sampled 300 via entrez): RS1001787573 (6:26215383 A>T), RS1002538521 (6:26216563 G>A,C), RS1002793227 (6:26217725 T>C), RS1002799030 (6:26216322 C>A,T), RS1006759405 (6:26217577 C>A,T), RS1007376861 (6:26214994 G>A,T), RS1010491655 (6:26215878 A>C,G,T), RS1011933595 (6:26215037 G>A,T), RS1012510149 (6:26217554 T>G), RS1012883659 (6:26217386 C>A,G,T), RS1013609205 (6:26217766 A>G), RS1014291705 (6:26215349 T>C), RS1014365317 (6:26215645 C>G), RS1014862039 (6:26217598 TA>T), RS1014881034 (6:26216139 T>C)

Disease associations

OMIM: gene MIM:602786 | disease phenotypes:

GenCC curated gene-disease

Mondo (0):

Orphanet (0):

HPO phenotypes

0 total (0 of 0 shown, HPO-id order):

GWAS associations

16 associations (top):

StudyTraitp-value
GCST004521_113Autism spectrum disorder or schizophrenia3.000000e-19
GCST004521_142Autism spectrum disorder or schizophrenia2.000000e-09
GCST004521_169Autism spectrum disorder or schizophrenia4.000000e-14
GCST004521_69Autism spectrum disorder or schizophrenia8.000000e-24
GCST004521_83Autism spectrum disorder or schizophrenia1.000000e-13
GCST007294_143Body fat distribution (trunk fat ratio)5.000000e-29
GCST007294_82Body fat distribution (trunk fat ratio)1.000000e-48
GCST007295_120Body fat distribution (leg fat ratio)2.000000e-46
GCST007295_91Body fat distribution (leg fat ratio)1.000000e-26
GCST010141_1Beef consumption7.000000e-13
GCST010143_19Meat-related diet5.000000e-13
GCST010143_31Meat-related diet7.000000e-09
GCST010143_5Meat-related diet4.000000e-09
GCST012226_43Waist circumference adjusted for body mass index4.000000e-13
GCST012227_893Hip circumference adjusted for BMI2.000000e-22
GCST90020028_935Hip circumference adjusted for BMI3.000000e-37

EFO canonical traits (4, from GWAS)

EFO IDTrait name
EFO:0004341body fat distribution
EFO:0008111diet measurement
EFO:0007789BMI-adjusted waist circumference
EFO:0008039BMI-adjusted hip circumference

Drugs & pharmacology

Drug and pharmacology data

Is drug target: no

PharmGKB: 1 entry (VIP=true, CPIC=false)

CTD chemical–gene interactions

51 total (human), top 30 by PubMed support.

ChemicalActions (top 5)PubMed papers
(+)-JQ1 compoundincreases expression, decreases expression5
Benzo(a)pyreneincreases expression3
Estradiolaffects expression, increases expression3
sodium arsenitedecreases expression2
Quercetindecreases expression, increases expression2
Silicon Dioxideincreases expression2
Tetrachlorodibenzodioxinincreases expression2
Cyclosporinedecreases expression, increases expression2
Cadmium Chlorideincreases abundance, increases expression2
urushioldecreases expression1
bisphenol Adecreases expression1
methylselenic aciddecreases expression1
2-methyl-4-isothiazolin-3-onedecreases expression1
thallium sulfatedecreases expression1
tris(1,3-dichloro-2-propyl)phosphatedecreases expression1
cobaltous chloridedecreases expression1
ferrous chlorideincreases expression1
2,3-bis(3’-hydroxybenzyl)butyrolactoneaffects cotreatment, decreases expression1
deguelinincreases expression1
2-palmitoylglycerolincreases expression1
fenpyroximateincreases expression1
4-chloro-N-((4-(1,1-dimethylethyl)phenyl)methyl)-3-ethyl-1-methyl-1H-pyrazole-5-carboxamideincreases expression1
dimethylarsinous acidincreases expression1
pyrimidifenincreases expression1
licochalcone Bincreases expression1
incobotulinumtoxinAdecreases expression1
Acetaminophenincreases expression1
Air Pollutantsincreases abundance, increases expression1
Berberinedecreases expression1
Cadmiumincreases abundance, increases expression1

Clinical trials (associated diseases)

0 trials via MONDO — disease-level, not drug-specific.

No linked Atlas pages yet — the cross-entity mesh grows as the corpus expands.