Skip to main content
Release 2026.08DMD context observedDMD candidate-conditioned prediction not yet eligible
View scientific status
Evidence freeze: 3 August 2026Resource: v1.2.0-measured-dmd-evidenceSchema: 1.1Open release status
Explore NMD-VCell

Stable server-rendered gene record · v1.2.0-measured-dmd-evidence

BET1

Inspect bounded evidence

G4 · muscle-context screen, not DMD replicationR0 · evidence annotation onlySupported · L1 resource recordAssessed · L3a external context screen

What this meansBET1 does not have an eligible observed perturbation in the current HepG2 release, but it has not been independently perturbed in a DMD muscle model. Different DMD datasets do not completely agree on its disease-associated direction. The next useful step is an experiment that closes the current evidence gap—not a therapeutic claim.

通俗解释BET1在当前HepG2数据中还没有合格的已观察扰动,但尚未在DMD肌肉模型中独立验证。不同DMD数据集对它的疾病相关方向并不完全一致。下一步应完成能弥补当前证据缺口的受控实验,而不能把它直接称为治疗靶点。

Design the next experiment →
Prediction readinessR0 · evidence annotation only
Current evidenceVersioned resource record; no eligible HepG2 perturbation
Additional contextAssessed · no current hit
Historical DMD prior (legacy)up
Source agreement2/4 sources

Gene Entity Page 2.1 · quantitative layer

Dataset-level evidence for BET1

Every row keeps its original context, metric and denominator. Empty fields remain explicit; no cross-source meta-effect is computed.

Download evidence JSON →
IdentityReleasedHGNC:14562 · ENSG00000105829
PerturbationNot assessedNo qualifying cell aggregate
Muscle contextScreen assessedExpression unavailable
DMD context4 source rowsDirectional conflict retained
DMD perturbation truthMissingNo independent DMD-muscle perturbation outcome
Calibrated predictionLockedR0 · no calibrated DMD response model
Dataset-level evidence rows for BET1
Dataset / evidenceContext and endpointObserved valueDenominator / supportState and source
GSE293514screen resultFusion-positive enrichmentHealthy human myoblast fusion CRISPR screen0.13164 log fold-changeFDR 0.9999991 contexts · 1 rows0 significant rowsassessed no hitOpen sourceHealthy-myoblast fusion endpoint only. A no-hit result is endpoint-specific and is not evidence of no muscle or DMD effect.
DMD single-cell baseline pseudobulkdisease context effectDisease-associated baseline expressionDMD skeletal-muscle single-cell source; baseline pseudobulk summaries0.405846 source-specific effect scaleMedian signed score 0.0000184819 contexts · 19 rows0 significant rowscontext onlyOpen sourceObserved-expression source summary; contextual evidence rather than candidate perturbation truth.
DMD single-cell delta / DIDdisease context effectDisease-associated change across declared contextsDMD skeletal-muscle single-cell source; final-label delta / DID summaries-0.141855 source-specific effect scaleMedian signed score -0.0000043720 contexts · 20 rows0 significant rowscontext onlyOpen sourceObserved-expression source summary; contextual evidence rather than candidate perturbation truth.
SEMA3C DESeq2 source-statedisease context effectSource-specific differential expressionDMD skeletal-muscle source-state analysis-0.124385 source-specific effect scaleMedian signed score -0.000019439 contexts · 9 rows0 significant rowscontext onlyOpen sourceObserved-expression source summary; contextual evidence rather than candidate perturbation truth.
SEMA3C NicheNet target-statedisease context effectInferred target-state relationshipDMD skeletal-muscle regulatory-inference context0.535134 source-specific effect scaleMedian signed score 0.032252762 contexts · 2 rows0 significant rowscontext onlyOpen sourceRegulatory-inference channel; displayed separately and not pooled as an independent expression cohort.

Source-specific effect display

DMD source-effect forest

Position is scaled to the largest absolute effect shown for this gene. Values remain on source-specific scales and are not pooled.

sc baseline pseudobulk+0.40584619 contexts · 0/19 significant rows
sc delta/DID-0.14185520 contexts · 0/20 significant rows
DESeq2 source-state-0.1243859 contexts · 0/9 significant rows
NicheNet target-state+0.5351342 contexts · 0/2 significant rows
independent dmd muscle perturbationmissing not negativeUnlock: Run an independent, quality-controlled perturbation in a declared DMD-relevant human myogenic model with biological replication.
per gene deg pathway and cell state profilenot published for this geneUnlock: Publish a per-gene inferential table with contrast, biological denominator, effect, uncertainty, multiplicity correction and provenance.
calibrated dmd response predictionlockedUnlock: Accumulate prospective DMD perturbation outcomes and pass the registered calibration, applicability and external-validation gates.

Dataset rows preserve their original context and scale. They are not pooled into a causal effect, therapeutic rank or calibrated DMD prediction.

Gene Entity Page 2.1

Entity graph: identity, evidence and prospective objects

This chain shows which objects exist for BET1, which are still drafts and which registries are empty. Empty is not a negative experimental result.

v1.2.0-measured-dmd-evidence
Object IDGENE:v1.2.0-measured-dmd-evidence:BET1
HGNCHGNC:14562
EnsemblENSG00000105829
NCBI Gene10282
Disease scopeDMD evidence context
01 · Gene objectRELEASEDStable identity and typed core record
02 · Evidence objectReleased record · no eligible perturbationNo DMD perturbation truth is implied
03 · Model gateR0 · R0 · evidence annotation onlyPredictionReadiness governance state
04 · Study objectNOT CREATEDNo candidate Study Card in this release
05 · Prediction objectEMPTYNo immutable prospective prediction
06 · Outcome objectEMPTYNo linked measured outcome

Claim boundary: object connectivity improves traceability; it does not raise the evidence tier or authorize a therapeutic claim.

Gene visual profile · 基因证据剖面

One-page evidence profile for BET1

A four-panel, descriptive view of the same bounded gene record: evidence depth, DMD source matrix, context gauges and the current decision gap. No score, target rank or prediction claim is computed.

a

Evidence profile

  1. L1 resourceStable record released
  2. L2 HepG2 perturbationnot assessed
  3. L3a external screenAssessed · no current hit
  4. L3b independent replicationNot assessed
  5. L4 DMD / muscle validationMissing
  6. L5 therapeutic / clinicalUnsupported
b

DMD source matrix

sc baseline pseudobulkPositive source directionMedian effect +0.405846 · signed score 0.00001848observed expression · 19 contexts · 0/19 significant rows
sc delta/DIDNegative source directionMedian effect -0.141855 · signed score -0.00000437observed expression · 20 contexts · 0/20 significant rows
DESeq2 source-stateNegative source directionMedian effect -0.124385 · signed score -0.00001943observed expression · 9 contexts · 0/9 significant rows
NicheNet target-statePositive source directionMedian effect +0.535134 · signed score 0.03225276regulatory inference · 2 contexts · 0/2 significant rows

Observed-expression and regulatory-inference channels are displayed side by side and are not pooled as independent cohorts.

c

Context gauges

Source agreement2/4 sources
This measures agreement among source pipelines; it is not biological ground truth.
Muscle expressionNot available
Visual guide; ≥1 TPM is the current triage threshold.
Cells contributing to the aggregateNot available
Coverage count, not a power calculation.
External screenAssessed · no current hit
This no-hit result is specific to the fusion-screen endpoint; it does not show that the gene has no muscle function.
d

Gap ladder

GAP-01Direct target-level perturbation evidence is absent
  1. Current actionInspect bounded evidence
  2. Highest missing layerL4 dmd functional validation
  3. Claim boundaryNo P1/P2 prediction claim unlocked

Interpretation boundary: this visual profile reorganizes frozen fields for inspection. It does not create a source-balanced successor result, a causal conclusion, a therapeutic direction or a clinical decision-support claim.

Decision boundary

What must be resolved next

Decision-blocking gapGAP-01 · Direct target-level perturbation evidence is absent
Highest missing layerL4 dmd functional validation
Readiness upgrade requiredAdd a governed perturbation response or direct disease-relevant experimental evidence.

The decision-blocking gap is the next missing layer that prevents the current action from advancing. The highest missing layer is the longer-term evidence ceiling; it is not necessarily the next experiment.

DMD context

Source-state record

DMD source-state fields for BET1
Direction stateconflicted
Variant stabilitynot assessed
Evidence modulesdirection conflicted
Statistical supportdirection only no significant context rows
Coverage4 of 4 sources
Uncertaintydirection conflict retained

Identifiers and context

Machine-resolvable core

Machine-resolvable identifiers and context for BET1
HGNCHGNC:14562
EnsemblENSG00000105829
NCBI Gene10282
HepG2 perturbationnot assessed
HepG2 observed cellsNot available
Observed counteralignmentNot available
Myoblast screenassessed
Myoblast fusion-screen effect0.13164 log fold-change
Myoblast fusion-screen FDR0.999999
Skeletal-muscle expressionNot available
DepMap median gene effectNot available

Cite this record

Stable identity

Object ID: GENE:v1.2.0-measured-dmd-evidence:BET1

NMD-VCell. BET1 evidence record. Resource v1.2.0-measured-dmd-evidence; evidence freeze 2026-08-03; schema 1.1; build EA-20260817-57. DOI pending.