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Release 2026.08DMD context observedDMD candidate-conditioned prediction not yet eligible
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Evidence freeze: 3 August 2026Resource: v1.2.0-measured-dmd-evidenceSchema: 1.1Open release status
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Stable server-rendered gene record · v1.2.0-measured-dmd-evidence

ACTN1

Inspect bounded evidence

G1 · DMD-background evidenceR0 · evidence annotation onlySupported · L1 resource recordAssessed · L1 resource record

What this meansACTN1 does not have an eligible observed perturbation in the current HepG2 release, but it has not been independently perturbed in a DMD muscle model. The available DMD source summaries should still be treated as contextual evidence rather than perturbation truth. The next useful step is an experiment that closes the current evidence gap—not a therapeutic claim.

通俗解释ACTN1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。现有DMD来源信息仍只是背景证据,不是扰动真值。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 contextNo qualifying external myogenic screen
Historical DMD prior (legacy)up
Source agreement4/4 sources

Gene Entity Page 2.1 · quantitative layer

Dataset-level evidence for ACTN1

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

Download evidence JSON →
IdentityReleasedHGNC:163 · ENSG00000072110
PerturbationNot assessedNo qualifying cell aggregate
Muscle contextScreen not assessedExpression unavailable
DMD context4 source rowsContextual source summaries
DMD perturbation truthMissingNo independent DMD-muscle perturbation outcome
Calibrated predictionLockedR0 · no calibrated DMD response model
Dataset-level evidence rows for ACTN1
Dataset / evidenceContext and endpointObserved valueDenominator / supportState and source
DMD single-cell baseline pseudobulkdisease context effectDisease-associated baseline expressionDMD skeletal-muscle single-cell source; baseline pseudobulk summaries0.100813 source-specific effect scaleMedian signed score 0.0000029520 contexts · 20 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 summaries0.007733 source-specific effect scaleMedian signed score 0.0000005820 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 analysis0.506875 source-specific effect scaleMedian signed score 0.003676859 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 context0.736081 source-specific effect scaleMedian signed score 0.039655462 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+0.10081320 contexts · 0/20 significant rows
sc delta/DID+0.00773320 contexts · 0/20 significant rows
DESeq2 source-state+0.5068759 contexts · 0/9 significant rows
NicheNet target-state+0.7360812 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 ACTN1, 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:ACTN1
HGNCHGNC:163
EnsemblENSG00000072110
NCBI Gene87
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 ACTN1

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 screenNot assessed
  4. L3b independent replicationNot assessed
  5. L4 DMD / muscle validationMissing
  6. L5 therapeutic / clinicalUnsupported
b

DMD source matrix

sc baseline pseudobulkPositive source directionMedian effect +0.100813 · signed score 0.00000295observed expression · 20 contexts · 0/20 significant rows
sc delta/DIDPositive source directionMedian effect +0.007733 · signed score 0.00000058observed expression · 20 contexts · 0/20 significant rows
DESeq2 source-statePositive source directionMedian effect +0.506875 · signed score 0.00367685observed expression · 9 contexts · 0/9 significant rows
NicheNet target-statePositive source directionMedian effect +0.736081 · signed score 0.03965546regulatory 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 agreement4/4 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 screenNot assessed
No qualifying evidence is available in this release; this is not a negative result.
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 ACTN1
Direction stateconsistent up
Variant stabilitynot assessed
Evidence modulesexploratory multisource core
Statistical supportdirection only no significant context rows
Coverage4 of 4 sources
Uncertaintydirection consistent not formal meta analysis

Identifiers and context

Machine-resolvable core

Machine-resolvable identifiers and context for ACTN1
HGNCHGNC:163
EnsemblENSG00000072110
NCBI Gene87
HepG2 perturbationnot assessed
HepG2 observed cellsNot available
Observed counteralignmentNot available
Myoblast screennot assessed
Myoblast fusion-screen effectNot available
Myoblast fusion-screen FDRNot available
Skeletal-muscle expressionNot available
DepMap median gene effectNot available

Cite this record

Stable identity

Object ID: GENE:v1.2.0-measured-dmd-evidence:ACTN1

NMD-VCell. ACTN1 evidence record. Resource v1.2.0-measured-dmd-evidence; evidence freeze 2026-08-03; schema 1.1; build EA-20260817-57. DOI pending.