Statements (25)
| Predicate | Object |
|---|---|
| gptkbp:instanceOf |
chromosomal band
|
| gptkbp:associatedWith |
gptkb:DiGeorge_syndrome
gptkb:velocardiofacial_syndrome |
| gptkbp:containsGene |
gptkb:LZTR1
gptkb:COMT gptkb:HIRA gptkb:DGCR8 gptkb:RTN4R CRKL TBX1 CLTCL1 PRODH ZDHHC8 |
| gptkbp:deletionSyndrome |
gptkb:22q11.2_deletion_syndrome
|
| gptkbp:genomicCoordinates |
chr22:18,800,000-21,500,000 (GRCh38)
|
| https://www.w3.org/2000/01/rdf-schema#label |
chromosome 22q11.21
|
| gptkbp:locatedOn |
chromosome 22
|
| gptkbp:locatedOnChromosome |
gptkb:22q11.21
|
| gptkbp:microdeletion |
22q11.21 microdeletion
|
| gptkbp:significance |
associated with psychiatric disorders
associated with congenital heart defects associated with immunodeficiency associated with palatal abnormalities |
| gptkbp:bfsParent |
gptkb:Nogo_receptor
|
| gptkbp:bfsLayer |
8
|