Statements (37)
| Predicate | Object |
|---|---|
| gptkbp:instanceOf |
chromosomal band
|
| gptkbp:associatedWith |
gptkb:DiGeorge_syndrome
gptkb:22q11.2_deletion_syndrome gptkb:velocardiofacial_syndrome |
| gptkbp:containsGene |
gptkb:LZTR1
gptkb:SNAP29 gptkb:CDC45 gptkb:COMT gptkb:HIRA gptkb:SLC25A1 gptkb:DGCR8 gptkb:RTN4R CRKL TBX1 CLTCL1 GP1BB PI4KA PRODH SEPT5 ZDHHC8 |
| gptkbp:genomicCoordinates |
chr22:18,800,000-21,500,000 (GRCh38)
|
| https://www.w3.org/2000/01/rdf-schema#label |
22q11.21
|
| gptkbp:locatedOn |
chromosome 22
|
| gptkbp:locatedOnChromosome |
gptkb:22q11.21
|
| gptkbp:significance |
congenital heart defects
immunodeficiency developmental delay psychiatric disorders hypocalcemia palatal abnormalities schizophrenia risk |
| gptkbp:bfsParent |
gptkb:LZTR1
gptkb:LZTR1_gene gptkb:CDC45 gptkb:SLC25A1 gptkb:DGCR8 |
| gptkbp:bfsLayer |
7
|