chromosomalLocation
P68690
predicate
Indicates the specific position or region on a chromosome where a genetic element (such as a gene or marker) is located.
All labels observed (7)
| Label | Occurrences |
|---|---|
| chromosomalLocation canonical | 12 |
| geneLocation | 1 |
| geneticLocusType | 1 |
| locatedOnChromosomeRegion | 1 |
| mappedToCytoband | 1 |
| mapsToCytogeneticBand | 1 |
| paralogLocation | 1 |
Description generation (PDg)
The one-sentence description above was generated by prompting gpt-5.1 with the predicate name and this instruction.
Instruction
Given a predicate that represents a relationship or action between entities, generate a one-sentence description explaining its meaning. # Instructions Focus on describing the relationship, not the entities themselves. # Response Format Begin the description with \' Indicates...\'
Input
Predicate: chromosomalLocation
Generated description
Indicates the specific position or region on a chromosome where a genetic element (such as a gene or marker) is located.
Sample triples (18)
| Subject | Object |
|---|---|
| FUS | 16p11.2 ⓘ |
| ABO blood group system | chromosome 9q34 ⓘ |
| bithorax complex | Drosophila 89E region via predicate surface "mapsToCytogeneticBand" NERFINISHED ⓘ |
| Antennapedia complex | complex locus via predicate surface "geneticLocusType" ⓘ |
| APOE ε3 allele | 19q13.32 via predicate surface "locatedOnChromosomeRegion" ⓘ |
| CYP1A2 | 15q24.1 ⓘ |
| BTK | Xq21.3–Xq22 ⓘ |
|
SMN1 gene
surface form:
SMN1
|
5q13.2 via predicate surface "paralogLocation" ⓘ |
| Gemin2 | human chromosome 14q21 ⓘ |
| HGNC:28350 | 9p21 via predicate surface "mappedToCytoband" ⓘ |
| catechol-O-methyltransferase | 22q11.21 (human COMT gene) ⓘ |
| tumor necrosis factor alpha | 6p21.33 ⓘ |
|
pregnane X receptor
surface form:
Pregnane X receptor
|
chromosome 3q13.33 ⓘ |
| CD46 | 1q32 ⓘ |
|
MAGL enzyme
surface form:
MAGL
|
human chromosome 3q21.3 ⓘ |
| interleukin-4 | human chromosome 5q31.1 ⓘ |
| Krabbe disease | chromosome 14q31 via predicate surface "geneLocation" ⓘ |
|
collie eye anomaly
surface form:
Collie eye anomaly
|
canine chromosome 37 ⓘ |