Statements (34)
| Predicate | Object |
|---|---|
| gptkbp:instanceOf |
gptkb:chromosomal_band
|
| gptkbp:arms |
acrocentric
|
| gptkbp:associatedWith |
gptkb:chronic_myelogenous_leukemia
gptkb:DiGeorge_syndrome gptkb:22q11.2_deletion_syndrome |
| gptkbp:containsCentromere |
yes
|
| gptkbp:containsGene |
gptkb:EP300
gptkb:NF2 gptkb:COMT gptkb:BCR gptkb:SMARCB1 gptkb:DGCR8 MYH9 SHANK3 |
| gptkbp:containsNucleolusOrganizerRegion |
yes
|
| gptkbp:foundIn |
gptkb:Homo_sapiens
|
| gptkbp:length |
approximately 51 million base pairs
|
| gptkbp:locatedOnChromosome |
22
|
| gptkbp:numberOfGenes |
~500
|
| gptkbp:orthologIn |
chromosome 22 (maternal)
chromosome 22 (paternal) |
| gptkbp:partOf |
human genome
|
| gptkbp:percentageOfTotalDNA |
about 1.5%
|
| gptkbp:region |
22q13
22q11.2 |
| gptkbp:sequencedIn |
1999
|
| gptkbp:bfsParent |
gptkb:TP53TG22
gptkb:chromosome_11_(mouse) gptkb:SCO2 gptkb:FBXO5_gene gptkb:SIF_(gene) gptkb:MAP3K49 |
| gptkbp:bfsLayer |
8
|
| https://www.w3.org/2000/01/rdf-schema#label |
human chromosome 22
|