Statements (15)
| Predicate | Object |
|---|---|
| gptkbp:instanceOf |
chromosomal band
|
| gptkbp:associatedWith |
16p12.2 microdeletion syndrome
|
| gptkbp:containsGene |
several protein-coding genes
|
| gptkbp:genomicCoordinates_(GRCh38) |
chr16:21,900,000-22,600,000
|
| gptkbp:genomicDisorder |
16p12.2 microdeletion
|
| https://www.w3.org/2000/01/rdf-schema#label |
16p12.2
|
| gptkbp:locatedOnChromosome |
gptkb:chromosome_16
short arm (p) of chromosome 16 |
| gptkbp:significance |
deletions associated with congenital anomalies
deletions associated with developmental delay deletions associated with intellectual disability |
| gptkbp:bfsParent |
gptkb:Partner_and_localizer_of_BRCA2_protein
gptkb:chromosome_16_(human) gptkb:PALB2 |
| gptkbp:bfsLayer |
7
|