H2BC6

gene
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Also known as H2B/hH2B.h

Summary

H2BC6 (H2B clustered histone 6, HGNC:4753) is a protein-coding gene on chromosome 6p22.2, encoding Histone H2B type 1-C/E/F/G/I (P62807). Core component of nucleosome. It is a common-essential gene (DepMap: required in 92.7% of cancer cell lines).

Histones are basic nuclear proteins that are responsible for the nucleosome structure of the chromosomal fiber in eukaryotes. Two molecules of each of the four core histones (H2A, H2B, H3, and H4) form an octamer, around which approximately 146 bp of DNA is wrapped in repeating units, called nucleosomes. The linker histone, H1, interacts with linker DNA between nucleosomes and functions in the compaction of chromatin into higher order structures. The protein has antibacterial and antifungal antimicrobial activity. This gene is intronless and encodes a replication-dependent histone that is a member of the histone H2B family. Transcripts from this gene lack polyA tails but instead contain a palindromic termination element. This gene is found in the large histone gene cluster on chromosome 6.

Source: NCBI Gene 8344 — RefSeq curated summary.

At a glance

  • GWAS associations: 38
  • Clinical variants (ClinVar): 29 total
  • Cancer dependency (DepMap): dependent in 92.7% of screened cell lines (common-essential)
  • MANE Select transcript: NM_003523

Identifiers

Gene identifiers

FieldValue
HGNC IDHGNC:4753
Approved symbolH2BC6
NameH2B clustered histone 6
Location6p22.2
Locus typegene with protein product
StatusApproved
AliasesH2B/h, H2B.h
Ensembl geneENSG00000274290
Ensembl biotypeprotein_coding
OMIM602805
Entrez8344

Gene structure

Transcript identifiers

Ensembl transcripts: 2 — 2 protein_coding

ENST00000614097, ENST00000634910

RefSeq mRNA: 1 — MANE Select: NM_003523 NM_003523

CCDS: CCDS4588

Canonical transcript exons

ENST00000614097 — 1 exons

ExonStartEnd
ENSE000037291772618376126184230

Expression profiles

Bgee: expression breadth ubiquitous, 208 present calls, max score 89.75.

FANTOM5 (CAGE): breadth ubiquitous, TPM avg 149.6724 / max 4752.1263, expressed in 1762 samples.

FANTOM5 promoters (2 alternative TSS)

Promoter IDTPM avgSamples expressed
66484147.24961637
664822.4228923

Top tissues by expression

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

TissueAnatomy IDExpression scoreQuality
adrenal tissueUBERON:001830389.75gold quality
tendon of biceps brachiiUBERON:000818889.31gold quality
endometrium epitheliumUBERON:000481185.67gold quality
bone marrow cellCL:000209285.32gold quality
tendonUBERON:000004382.54gold quality
heart right ventricleUBERON:000208081.68silver quality
male germ line stem cell (sensu Vertebrata) in testisCL:0000089 ∩ UBERON:000047381.03gold quality
calcaneal tendonUBERON:000370180.89gold quality
oocyteCL:000002379.60silver quality
colonic epitheliumUBERON:000039778.01gold quality
cartilage tissueUBERON:000241877.59gold quality
bone marrowUBERON:000237177.50gold quality
thymusUBERON:000237077.00silver quality
medial globus pallidusUBERON:000247776.82silver quality
corpus epididymisUBERON:000435976.54gold quality
bronchial epithelial cellCL:000232874.19gold quality
amniotic fluidUBERON:000017373.84gold quality
jejunal mucosaUBERON:000039973.35gold quality
upper leg skinUBERON:000426273.25gold quality
oviduct epitheliumUBERON:000480472.77silver quality
bloodUBERON:000017872.76gold quality
oral cavityUBERON:000016771.83silver quality
secondary oocyteCL:000065571.77silver quality
deciduaUBERON:000245071.37silver quality
globus pallidusUBERON:000187571.29silver quality
trabecular bone tissueUBERON:000248370.98silver quality
embryoUBERON:000092270.96gold quality
placentaUBERON:000198770.96gold quality
colonic mucosaUBERON:000031770.76silver quality
tonsilUBERON:000237270.69gold quality

Single-cell (SCXA)

Detected in 1 experiment(s), a significant marker in 0.

ExperimentMarker?Max mean expression
E-ANND-3no2.95

Regulation

Is transcription factor: no

Functional genomics

DepMap (CRISPR cell-line fitness): dependent in 92.7% of screened cell lines, common-essential.

Literature-anchored findings (GeneRIF, showing 1)

  • Histone H2B antimicrobial peptides participate in the colonic defense against bacteria and fungi. (PMID:12860195)

Cross-species orthologs

3 orthologs

OrganismSymbolGene ID
mus_musculusH2bc4ENSMUSG00000018102
mus_musculusH2bc6ENSMUSG00000047246
rattus_norvegicusHist1h2bcENSRNOG00000069373

Paralogs (21): H2BW2 (ENSG00000101812), H2BW1 (ENSG00000123569), H2BC11 (ENSG00000124635), H2BC1 (ENSG00000146047), H2BC5 (ENSG00000158373), H2BC4 (ENSG00000180596), H2BC21 (ENSG00000184678), H2BC13 (ENSG00000185130), H2BC26 (ENSG00000196890), H2BC12 (ENSG00000197903), H2BC18 (ENSG00000203814), H2BC15 (ENSG00000233822), H2BC12L (ENSG00000234289), H2BC14 (ENSG00000273703), H2BC8 (ENSG00000273802), H2BC17 (ENSG00000274641), H2BC9 (ENSG00000275713), H2BC3 (ENSG00000276410), H2BC7 (ENSG00000277224), H2BC10 (ENSG00000278588), H2BK1 (ENSG00000285480)

Protein

Protein identifiers

Histone H2B type 1-C/E/F/G/IP62807 (reviewed: P62807)

Alternative names: Histone H2B.1 A, Histone H2B.a, Histone H2B.g, Histone H2B.h, Histone H2B.k, Histone H2B.l

All UniProt accessions (2): P62807, B2R4S9

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. Has broad antibacterial activity. May contribute to the formation of the functional antimicrobial barrier of the colonic epithelium, and to the bactericidal activity of amniotic fluid.

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. Interacts with VRK1; the interaction is mediated by the nucleosome acidic patch, a cluster of negatively charged residues of H2A and H2B forming a cleft within the nucleosome core.

Subcellular location. Nucleus. Chromosome.

Post-translational modifications. Monoubiquitination at Lys-35 (H2BK34Ub) by the MSL1/MSL2 dimer is required for histone H3 ‘Lys-4’ (H3K4me) and ‘Lys-79’ (H3K79me) methylation and transcription activation at specific gene loci, such as HOXA9 and MEIS1 loci. Similarly, monoubiquitination at Lys-121 (H2BK120Ub) by the RNF20/40 complex gives a specific tag for epigenetic transcriptional activation and is also prerequisite for histone H3 ‘Lys-4’ and ‘Lys-79’ methylation. It also functions cooperatively with the FACT dimer to stimulate elongation by RNA polymerase II. H2BK120Ub also acts as a regulator of mRNA splicing: deubiquitination by USP49 is required for efficient cotranscriptional splicing of a large set of exons. Phosphorylation at Ser-37 (H2BS36ph) by AMPK in response to stress promotes transcription. Phosphorylated on Ser-15 (H2BS14ph) by STK4/MST1 during apoptosis; which facilitates apoptotic chromatin condensation. Also phosphorylated on Ser-15 in response to DNA double strand breaks (DSBs), and in correlation with somatic hypermutation and immunoglobulin class-switch recombination. GlcNAcylation at Ser-113 promotes monoubiquitination of Lys-121. It fluctuates in response to extracellular glucose, and associates with transcribed genes. ADP-ribosylated by PARP1 or PARP2 on Ser-7 (H2BS6ADPr) in response to DNA damage. H2BS6ADPr promotes recruitment of CHD1L. Mono-ADP-ribosylated on Glu-3 (H2BE2ADPr) by PARP3 in response to single-strand breaks. Poly ADP-ribosylation on Glu-36 (H2BE35ADPr) by PARP1 regulates adipogenesis: it inhibits phosphorylation at Ser-37 (H2BS36ph), thereby blocking expression of pro-adipogenetic genes. 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 H2B family.

RefSeq proteins (1): NP_003514* (*=MANE)

Domains & families (InterPro)

IDNameType
IPR000558Histone_H2BFamily
IPR007125H2A/H2B/H3Domain
IPR009072Histone-foldHomologous_superfamily
IPR055333HISTONE_H2B_siteConserved_site

Pfam: PF00125

UniProt features (110 total): modified residue 91, helix 4, cross-link 4, sequence conflict 2, strand 2, initiator methionine 1, chain 1, sequence variant 1, mutagenesis site 1, region of interest 1, compositionally biased region 1, glycosylation site 1

Structure

Experimental structures (PDB)

76 structures, top 30 by resolution.

PDBMethodResolution (Å)
6ACOX-RAY DIFFRACTION1.71
7R5RELECTRON MICROSCOPY2.44
8OX0ELECTRON MICROSCOPY2.52
9Y46ELECTRON MICROSCOPY2.59
10XZELECTRON MICROSCOPY2.6
7PIIELECTRON MICROSCOPY2.68
7U46ELECTRON MICROSCOPY2.68
10YAELECTRON MICROSCOPY2.7
10YCELECTRON MICROSCOPY2.7
8OOPELECTRON MICROSCOPY2.7
8OX1ELECTRON MICROSCOPY2.7
9Y47ELECTRON MICROSCOPY2.74
10YBELECTRON MICROSCOPY2.8
10YDELECTRON MICROSCOPY2.8
8OO7ELECTRON MICROSCOPY2.8
5GT0X-RAY DIFFRACTION2.82
6X59ELECTRON MICROSCOPY2.98
7TANELECTRON MICROSCOPY3
8VWUELECTRON MICROSCOPY3
6SEGELECTRON MICROSCOPY3.1
7U51ELECTRON MICROSCOPY3.1
8QZMELECTRON MICROSCOPY3.1
8VWSELECTRON MICROSCOPY3.1
9DWFELECTRON MICROSCOPY3.1
9EOZELECTRON MICROSCOPY3.1
7A08ELECTRON MICROSCOPY3.11
9NQUELECTRON MICROSCOPY3.16
8OOAELECTRON MICROSCOPY3.18
7UV9ELECTRON MICROSCOPY3.2
8X15ELECTRON MICROSCOPY3.2

Predicted structure (AlphaFold)

ModelpLDDTFraction very-high
AF-P62807-F187.940.68

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 (95): 6, 6, 6, 6, 7, 12, 12, 12, 12, 12, 12, 13, 13, 13, 15, 16, 16, 16, 16, 17 …

Glycosylation sites (1): 113

Mutagenesis-validated functional residues (1):

PositionPhenotype
114no effect on interaction with vrk1.

Function

Pathways and Gene Ontology

Reactome pathways

58 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-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-5689880Ub-specific processing proteases
R-HSA-5693565Recruitment and ATM-mediated phosphorylation of repair and signaling proteins at DNA double strand breaks
R-HSA-5693571Nonhomologous End-Joining (NHEJ)
R-HSA-5693607Processing of DNA double-strand break ends
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-69473G2/M DNA damage checkpoint

MSigDB gene sets: 222 (showing top): REACTOME_MEIOTIC_RECOMBINATION, REACTOME_DNA_REPLICATION, REACTOME_SIGNALING_BY_NOTCH, GOBP_ANTIMICROBIAL_HUMORAL_RESPONSE, CHIARADONNA_NEOPLASTIC_TRANSFORMATION_KRAS_DN, RODRIGUES_THYROID_CARCINOMA_POORLY_DIFFERENTIATED_UP, REACTOME_ADAPTIVE_IMMUNE_SYSTEM, REACTOME_MEIOTIC_SYNAPSIS, REACTOME_G2_M_DNA_DAMAGE_CHECKPOINT, GRAESSMANN_APOPTOSIS_BY_DOXORUBICIN_UP, GRAESSMANN_RESPONSE_TO_MC_AND_DOXORUBICIN_UP, GOBP_ORGAN_OR_TISSUE_SPECIFIC_IMMUNE_RESPONSE, REACTOME_ADHERENS_JUNCTIONS_INTERACTIONS, GERY_CEBP_TARGETS, GOBP_DEFENSE_RESPONSE_TO_OTHER_ORGANISM

GO Biological Process (6): innate immune response in mucosa (GO:0002227), nucleosome assembly (GO:0006334), antibacterial humoral response (GO:0019731), defense response to Gram-positive bacterium (GO:0050830), antimicrobial humoral immune response mediated by antimicrobial peptide (GO:0061844), defense response to bacterium (GO:0042742)

GO Molecular Function (5): DNA binding (GO:0003677), structural constituent of chromatin (GO:0030527), identical protein binding (GO:0042802), protein heterodimerization activity (GO:0046982), protein binding (GO:0005515)

GO Cellular Component (7): nucleosome (GO:0000786), obsolete extracellular space (GO:0005615), nucleus (GO:0005634), nucleoplasm (GO:0005654), cytosol (GO:0005829), extracellular exosome (GO:0070062), chromosome (GO:0005694)

Reactome top-level categories

Rollup of top-12 pathways:

CategoryPathways
Cellular Senescence3
Depyrimidination2
Depurination2
Epigenetic regulation of gene expression2
Chromatin modifying enzymes2
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
Mitotic Prophase1

GO top-level categories

Rollup of top GO terms by namespace:

CategoryTerms
antimicrobial humoral response2
defense response to bacterium2
chromatin2
cellular anatomical structure2
mucosal immune response1
innate immune response1
chromatin organization1
nucleosome organization1
protein-DNA complex assembly1
defense response1
response to bacterium1
nucleic acid binding1
structural molecule activity1
protein binding1
protein dimerization activity1
binding1
protein-DNA complex1
intracellular membrane-bounded organelle1
nuclear lumen1
cytoplasm1
extracellular vesicle1
intracellular membraneless organelle1

Protein interactions and networks

STRING

0 interactions, top by confidence (×1000):

IntAct

113 interactions, top by confidence:

ABTypeScore
H2AZ1ZNHIT1psi-mi:“MI:0914”(association)0.770
ANP32EH2AZ1psi-mi:“MI:0914”(association)0.770
ANP32EH2AZ1psi-mi:“MI:0915”(physical association)0.770
TP53BP1H2AC11psi-mi:“MI:0915”(physical association)0.670
H2AC11UBBpsi-mi:“MI:0915”(physical association)0.650
MAPK7PFDN6psi-mi:“MI:0914”(association)0.640
HIP1HIP1Rpsi-mi:“MI:0914”(association)0.640
FHH2AZ1psi-mi:“MI:0914”(association)0.620
H2BC10TP53BP2psi-mi:“MI:0915”(physical association)0.560
H2BC10AP2M1psi-mi:“MI:0915”(physical association)0.560

BioGRID (1779): HIST1H2BC (Two-hybrid), HIST1H2BG (Affinity Capture-RNA), HIST1H2BG (Affinity Capture-RNA), HIST1H2BD (Affinity Capture-MS), HIST1H2BD (Affinity Capture-MS), HIST1H2BD (Reconstituted Complex), HIST1H2BG (Reconstituted Complex), HIST1H2BF (Reconstituted Complex), HIST1H2BE (Reconstituted Complex), HIST1H2BI (Reconstituted Complex), HIST1H2BC (Reconstituted Complex), TPX2 (Proximity Label-MS), SMCHD1 (Proximity Label-MS), KIF23 (Proximity Label-MS), KIF4A (Proximity Label-MS)

ESM2 similar proteins: A0A2R8Y619, O97484, P02284, P02285, P02286, P02287, P02288, P04255, P04913, P07794, P07795, P0C1H4, P16888, P16889, P16890, P19374, P21897, P23527, P27326, P30757, P33778, P35067, P35068, P35069, P48557, P57053, P62807, P62808, P70696, P83863, Q00715, Q00729, Q16778, Q27894, Q32L48, Q5QNW6, Q5R893, Q5RCP8, Q64475, Q64478

Diamond homologs: A0A2R8Y619, A2WKT1, A2WKT4, A2WWU2, A2XF66, A2YWI3, A3AGM4, O22582, O60814, O65819, P02281, P02283, P02284, P02285, P02286, P02287, P02288, P02289, P02290, P04255, P06145, P06899, P06900, P07794, P07795, P0C1H3, P0C1H4, P0C1H5, P10853, P10854, P14001, P16888, P16889, P16890, P17271, P19374, P21897, P23527, P27326, P27807

SIGNOR signaling

2 interactions.

AEffectBMechanism
SLBP“up-regulates quantity by expression”H2BC4“translation regulation”
“MSL acetyltransferase”“down-regulates activity”H2BC4monoubiquitination

Enriched among interaction partners

Reactome pathways and GO biological processes over-represented among this gene’s 101 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
Activation of NF-kappaB in B cells512.6×5e-03
Signaling by ALK fusions and activated point mutants611.6×2e-03
Recruitment and ATM-mediated phosphorylation of repair and signaling proteins at DNA double strand breaks611.3×2e-03
Deposition of new CENPA-containing nucleosomes at the centromere510.2×8e-03
B-WICH complex positively regulates rRNA expression69.3×5e-03
Oxidative Stress Induced Senescence89.3×1e-03
Senescence-Associated Secretory Phenotype (SASP)78.9×2e-03
Processing of DNA double-strand break ends68.8×5e-03

GO biological processes:

GO termPartnersFoldFDR
heterochromatin formation515.0×3e-03
chromatin remodeling119.4×1e-05
regulation of apoptotic process98.8×2e-04
negative regulation of apoptotic process114.5×3e-03

Disease & clinical

Clinical variants and AI predictions

ClinVar

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

ClassificationCount (floor)
Pathogenic0
Likely pathogenic0
Uncertain significance28
Likely benign1
Benign0

Top pathogenic / likely-pathogenic (0)

SpliceAI

502 predictions. Top by Δscore:

VariantEffectΔscore
6:26183280:C:CAacceptor_gain0.9800
6:26172608:G:GTdonor_gain0.9700
6:26183280:C:Gacceptor_gain0.9700
6:26172231:A:AGdonor_gain0.9600
6:26172783:GT:Gdonor_gain0.9600
6:26183279:AC:Aacceptor_gain0.9600
6:26183780:GAACA:Gacceptor_gain0.9600
6:26172173:G:GTdonor_gain0.9500
6:26172601:GA:Gdonor_gain0.9500
6:26172700:A:Gdonor_gain0.9500
6:26183252:G:Cacceptor_gain0.9400
6:26172533:C:Tdonor_gain0.9300
6:26172603:G:GGdonor_gain0.9300
6:26183779:A:AGacceptor_gain0.9300
6:26183780:G:GGacceptor_gain0.9300
6:26183780:GAAC:Gacceptor_gain0.9300
6:26172224:GCCT:Gdonor_gain0.9200
6:26172789:G:GGdonor_gain0.9200
6:26172200:G:GTdonor_gain0.9100
6:26172693:GCT:Gdonor_gain0.9100
6:26172092:G:GAdonor_gain0.9000
6:26172777:G:Tdonor_gain0.9000
6:26183250:C:CAacceptor_gain0.9000
6:26172665:G:Tdonor_gain0.8900
6:26172326:G:GGdonor_gain0.8800
6:26183780:GA:Gacceptor_gain0.8800
6:26172217:G:GAdonor_gain0.8700
6:26172665:G:GTdonor_gain0.8700
6:26172785:GTAT:Gdonor_gain0.8700
6:26173622:T:Gdonor_gain0.8700

AlphaMissense

0 scored. Top likely-pathogenic:

dbSNP variants (sampled 300 via entrez): RS1002852454 (6:26182959 A>C), RS1002911379 (6:26183954 C>G,T), RS1005520740 (6:26184464 A>G), RS1007404959 (6:26181973 G>C), RS1007478573 (6:26182537 CCT>C), RS1007776448 (6:26182304 G>A,C), RS1008186138 (6:26184507 G>A), RS1008443564 (6:26184351 ACT>A), RS1008826790 (6:26183615 A>G), RS1009036890 (6:26183541 C>G,T), RS1009468740 (6:26181782 G>A), RS1009807805 (6:26183508 G>A,C), RS1009862251 (6:26183279 A>C), RS1010377939 (6:26182878 G>A), RS1010471436 (6:26183199 G>C)

Disease associations

OMIM: gene MIM:602805 | disease phenotypes:

GenCC curated gene-disease

Mondo (0):

Orphanet (0):

HPO phenotypes

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

GWAS associations

38 associations (top):

StudyTraitp-value
GCST004212_19Height3.000000e-13
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
GCST005146_45Birth weight1.000000e-08
GCST006426_3Serum urate levels in chronic kidney disease9.000000e-07
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
GCST007325_267General risk tolerance (MTAG)9.000000e-14
GCST008163_299Height1.000000e-18
GCST008163_41Height5.000000e-06
GCST008362_109Birth weight2.000000e-06
GCST008362_151Birth weight1.000000e-13
GCST008363_111Offspring birth weight2.000000e-08
GCST010002_50Refractive error4.000000e-34
GCST010141_1Beef consumption7.000000e-13
GCST010142_16Fish- and plant-related diet2.000000e-10
GCST010142_19Fish- and plant-related diet4.000000e-10
GCST010142_34Fish- and plant-related diet7.000000e-09
GCST010142_35Fish- and plant-related diet8.000000e-09
GCST010142_42Fish- and plant-related diet1.000000e-08
GCST010142_7Fish- and plant-related diet3.000000e-12
GCST010143_19Meat-related diet5.000000e-13
GCST010143_31Meat-related diet7.000000e-09
GCST010143_5Meat-related diet4.000000e-09
GCST010702_75Subcortical volume (MOSTest)3.000000e-11

EFO canonical traits (10, from GWAS)

EFO IDTrait name
EFO:0004344birth weight
EFO:0004531urate measurement
EFO:0004341body fat distribution
EFO:0008579risk-taking behaviour
EFO:0005939parental genotype effect measurement
EFO:0008111diet measurement
EFO:0004346neuroimaging measurement
EFO:0007789BMI-adjusted waist circumference
EFO:0008039BMI-adjusted hip circumference
EFO:0004980appendicular lean mass

Drugs & pharmacology

Drug and pharmacology data

Is drug target: no

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

CTD chemical–gene interactions

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

ChemicalActions (top 5)PubMed papers
propionaldehydedecreases expression, increases methylation2
bisphenol Adecreases expression, increases expression2
Silicon Dioxideincreases expression2
Aflatoxin B1increases methylation, increases expression2
Copper Sulfateincreases expression, decreases expression2
nonanalincreases methylation1
n-hexanalincreases methylation1
butyraldehydeincreases methylation1
caprylic aldehydeincreases methylation1
N,N,N’,N’-tetrakis(2-pyridylmethyl)ethylenediamineincreases expression1
pentanalincreases methylation1
heptanalincreases methylation1
licochalcone Bincreases expression1
jinfukangaffects cotreatment, decreases expression1
NSC 689534increases expression, affects binding1
(+)-JQ1 compoundincreases expression1
Resveratrolincreases expression1
Acetaminophenincreases expression1
Air Pollutantsincreases abundance, increases expression1
Amiodaroneincreases expression1
Benzo(a)pyrenedecreases methylation1
Berberinedecreases expression1
Cisplatinaffects cotreatment, decreases expression1
Copperaffects binding, increases expression1
Coumestroldecreases expression1
Dichlorodiphenyl Dichloroethylenedecreases expression1
Demecolcineincreases expression1
Dimethyl Sulfoxideaffects expression1
Doxorubicindecreases expression1
Formaldehydeincreases 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.