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pat-6

C. elegans

Paralyzed arrest at two-fold protein 6

What the model saw

Gene: pat-6
Organism: Caenorhabditis elegans
Known functions: Paralyzed arrest at two-fold protein 6. actin binding. protein binding.
View unredacted entry
Paralyzed arrest at two-fold protein 6. actin binding. protein binding.

Solver output

Predicted influence
Unclear
Confidence
35%
Mechanism
Other
Reasoning

pat-6 (Paralyzed Arrest at Two-fold protein 6) is a C. elegans actopaxin/parvin ortholog that functions as an actin-binding and protein-binding component of integrin adhesion complexes, linking integrins to the actin cytoskeleton at muscle attachment sites. Its primary role is in muscle integrity and mechanotransduction rather than in canonical longevity-regulating pathways such as insulin/IGF-1 signaling, TOR, or mitochondrial function. While cytoskeletal integrity and proteostasis can intersect with aging, the molecular function annotations (actin binding, protein binding in the context of integrin-linked kinase complexes) do not clearly map to a pro- or anti-longevity mechanism. Loss of pat-6 causes embryonic/larval paralysis and arrest, reflecting a structural role rather than a direct modulator of lifespan pathways, making the longevity influence genuinely ambiguous from these annotations alone.

Key pathways
integrin-actin cytoskeleton linkagemuscle attachment complex / integrin adhesionmechanotransduction
Longevity influence
Anti-longevity
Lifespan effect
Increase

GenAge curators classify each gene's normal function as promoting (Pro-Longevity) or opposing (Anti-Longevity) longevity, based on synthesis across studies. Loss-of-function effects can vary from this depending on the manipulation.

Advisor judgment

Answer
Incorrect
Mechanism
Incorrect
Reasoning quality
3/5
Failure mode
Appropriately uncertain
Notes

The model predicted "unclear" with low confidence (0.35), while the ground truth is "anti_longevity." The model's reasoning about pat-6's role in integrin adhesion complexes and muscle integrity is mechanistically reasonable, but it failed to commit to the correct anti-longevity classification. The model correctly identified the gene's structural/cytoskeletal role but did not connect this to an anti-longevity effect (where loss of function might extend lifespan by reducing proteotoxic stress or through other mechanisms). The reasoning quality is moderate - the model showed good knowledge of the gene's biology but was overly cautious in its final classification. This is a case of appropriate uncertainty rather than confident wrongness, but the answer is still incorrect.

Raw API responses

solver

{
  "reasoning": "pat-6 (Paralyzed Arrest at Two-fold protein 6) is a C. elegans actopaxin/parvin ortholog that functions as an actin-binding and protein-binding component of integrin adhesion complexes, linking integrins to the actin cytoskeleton at muscle attachment sites. Its primary role is in muscle integrity and mechanotransduction rather than in canonical longevity-regulating pathways such as insulin/IGF-1 signaling, TOR, or mitochondrial function. While cytoskeletal integrity and proteostasis can intersect with aging, the molecular function annotations (actin binding, protein binding in the context of integrin-linked kinase complexes) do not clearly map to a pro- or anti-longevity mechanism. Loss of pat-6 causes embryonic/larval paralysis and arrest, reflecting a structural role rather than a direct modulator of lifespan pathways, making the longevity influence genuinely ambiguous from these annotations alone.",
  "confidence": 0.35,
  "key_pathways": [
    "integrin-actin cytoskeleton linkage",
    "muscle attachment complex / integrin adhesion",
    "mechanotransduction"
  ],
  "mechanism_class": "other",
  "longevity_influence": "unclear"
}

advisor

{
  "notes": "The model predicted \"unclear\" with low confidence (0.35), while the ground truth is \"anti_longevity.\" The model's reasoning about pat-6's role in integrin adhesion complexes and muscle integrity is mechanistically reasonable, but it failed to commit to the correct anti-longevity classification. The model correctly identified the gene's structural/cytoskeletal role but did not connect this to an anti-longevity effect (where loss of function might extend lifespan by reducing proteotoxic stress or through other mechanisms). The reasoning quality is moderate - the model showed good knowledge of the gene's biology but was overly cautious in its final classification. This is a case of appropriate uncertainty rather than confident wrongness, but the answer is still incorrect.",
  "failure_mode": "appropriately_uncertain",
  "answer_correct": false,
  "mechanism_correct": false,
  "reasoning_quality": 3,
  "ground_truth_questionable": false
}
pat-6 · Caenorhabditis elegans | Aging biology eval