Statements (18)
| Predicate | Object |
|---|---|
| gptkbp:instanceOf |
gptkb:chromosomal_band
|
| gptkbp:associatedWith |
gptkb:Parkinson's_disease
gptkb:Koolen–de_Vries_syndrome frontotemporal dementia |
| gptkbp:associatedWithHaploinsufficiency |
gptkb:KANSL1
|
| gptkbp:associatedWithInversionPolymorphism |
17q21.31 inversion
|
| gptkbp:associatedWithMicrodeletionSyndrome |
17q21.31 microdeletion syndrome
|
| gptkbp:containsGene |
gptkb:NSF
gptkb:MAPT gptkb:CRHR1 gptkb:KANSL1 gptkb:PLEKHM1 |
| gptkbp:genomeAssemblyReference |
gptkb:GRCh38
|
| gptkbp:locatedOnChromosome |
gptkb:chromosome_17
17q21.31 |
| gptkbp:bfsParent |
gptkb:NSF_(N-ethylmaleimide-sensitive_factor)
|
| gptkbp:bfsLayer |
7
|
| http://www.w3.org/2000/01/rdf-schema#label |
17q21.31 (human)
|