Statements (27)
| Predicate | Object |
|---|---|
| gptkbp:instanceOf |
chromosomal band
|
| gptkbp:associatedWith |
1q21.1 deletion syndrome
1q21.1 duplication syndrome |
| gptkbp:containsGene |
gptkb:PRKAB2
gptkb:GJA5 gptkb:PDZK1 CHD1L HYDIN2 NBPF family genes RBM8A |
| gptkbp:hasGenomicCoordinates |
chr1:146,000,000-148,000,000 (approximate)
|
| https://www.w3.org/2000/01/rdf-schema#label |
1q21.1
|
| gptkbp:locatedOn |
chromosome 1
|
| gptkbp:locatedOnChromosome |
gptkb:1q21.1
|
| gptkbp:significance |
gptkb:autism_spectrum_disorder
schizophrenia congenital heart defects intellectual disability neurodevelopmental disorders macrocephaly microcephaly |
| gptkbp:subjectOf |
clinical genetics
genomic research |
| gptkbp:bfsParent |
gptkb:PRKAB2
gptkb:POLR3C_gene gptkb:SLC40A1 |
| gptkbp:bfsLayer |
7
|