mutationAssociatedWith
P68687
predicate
Indicates that a specific genetic mutation is linked or related to another entity, such as a disease, trait, or molecular effect.
Observed surface forms (6)
- polymorphismAssociatedWith ×5
- mutationCause ×4
- causedByMutationIn ×3
- mutation ×3
- mutationTypeAssociatedWithDisease ×3
- mutationCauses ×1
Sample triples (24)
| Subject | Object |
|---|---|
| CYP1A2 | risk of adverse drug reactions via predicate surface "polymorphismAssociatedWith" ⓘ |
| CYP1A2 | variation in caffeine metabolism via predicate surface "polymorphismAssociatedWith" ⓘ |
| CYP1A2 | variation in drug response via predicate surface "polymorphismAssociatedWith" ⓘ |
| Clone Force 99 | enhanced intellect (Tech) via predicate surface "mutation" ⓘ |
| Clone Force 99 | enhanced marksmanship (Crosshair) via predicate surface "mutation" ⓘ |
| Clone Force 99 | enhanced strength (Wrecker) via predicate surface "mutation" ⓘ |
|
HTT gene
surface form:
HTT
|
Huntington's disease via predicate surface "mutationCauses" NERFINISHED ⓘ |
|
INS gene in humans
surface form:
INS gene
|
birth weight variation via predicate surface "polymorphismAssociatedWith" ⓘ |
|
INS gene in humans
surface form:
INS gene
|
type 1 diabetes risk via predicate surface "polymorphismAssociatedWith" ⓘ |
| Krabbe disease | GALC gene via predicate surface "causedByMutationIn" NERFINISHED ⓘ |
| Purple Tentacle | toxic sludge via predicate surface "mutationCause" ⓘ |
|
Reapers
surface form:
Reapers (Blade universe)
|
genetic engineering via predicate surface "mutationCause" ⓘ |
|
Reapers
surface form:
Reapers (Blade universe)
|
vampire experimentation via predicate surface "mutationCause" ⓘ |
|
SMN1 gene
surface form:
SMN1
|
gene conversion to SMN2 via predicate surface "mutationTypeAssociatedWithDisease" ⓘ |
|
SMN1 gene
surface form:
SMN1
|
homozygous deletion via predicate surface "mutationTypeAssociatedWithDisease" ⓘ |
|
SMN1 gene
surface form:
SMN1
|
point mutation via predicate surface "mutationTypeAssociatedWithDisease" ⓘ |
| TARDBP | familial ALS ⓘ |
| TARDBP | sporadic ALS ⓘ |
|
The Family
surface form:
The Family (The Omega Man)
|
biological warfare plague via predicate surface "mutationCause" ⓘ |
| cytochrome P450 reductase | Antley–Bixler syndrome (POR-related) NERFINISHED ⓘ |
| cytochrome P450 reductase | POR deficiency ⓘ |
| cytochrome P450 reductase | disorders of steroidogenesis ⓘ |
| tuberous sclerosis complex | TSC1 gene via predicate surface "causedByMutationIn" NERFINISHED ⓘ |
| tuberous sclerosis complex | TSC2 gene via predicate surface "causedByMutationIn" NERFINISHED ⓘ |