Statements (43)
| Predicate | Object |
|---|---|
| gptkbp:instanceOf |
chromosomal band
|
| gptkbp:associatedWith |
gptkb:Wilms_tumor
gptkb:sickle_cell_anemia gptkb:Alport_syndrome gptkb:Beckwith-Wiedemann_syndrome beta thalassemia congenital adrenal hyperplasia |
| gptkbp:autosome |
true
|
| gptkbp:bandingPattern |
11p, 11q
|
| gptkbp:centromerePosition |
metacentric
|
| gptkbp:containsGene |
gptkb:SLC22A5
gptkb:FADD gptkb:HBB gptkb:SLC22A4 gptkb:WT1 gptkb:APOA1 gptkb:CST3 gptkb:FEN1 gptkb:DRD4 gptkb:INS gptkb:KCNQ1 gptkb:CD44 gptkb:MMP13 gptkb:TYR gptkb:PAX6 TRIM5 PCSK7 SAA1 SAA2 SAA4 |
| gptkbp:Entrez_Gene_ID |
ENSG000001
|
| https://www.w3.org/2000/01/rdf-schema#label |
chromosome 11 (human)
|
| gptkbp:length |
135 million base pairs
|
| gptkbp:locatedOnChromosome |
11
|
| gptkbp:numberOfGenes |
~1350
|
| gptkbp:OMIMEntry |
#215100
|
| gptkbp:organism |
gptkb:Homo_sapiens
|
| gptkbp:partOf |
human genome
|
| gptkbp:RefSeq |
NC_000011.10
|
| gptkbp:bfsParent |
gptkb:chromosome_9_(mouse)
gptkb:miR-192 gptkb:Myod1 |
| gptkbp:bfsLayer |
7
|