|
gptkbp:instanceOf
|
chromosomal band
|
|
gptkbp:associatedWith
|
gptkb:hereditary_diffuse_gastric_cancer
gptkb:tuberous_sclerosis
gptkb:Crohn's_disease
gptkb:alpha-thalassemia
gptkb:familial_Mediterranean_fever
polycystic kidney disease
|
|
gptkbp:centromere_position
|
submetacentric
|
|
gptkbp:containsGene
|
gptkb:TSC2
gptkb:CREBBP
gptkb:MC1R
gptkb:HBA1
gptkb:HBA2
gptkb:CDH1
gptkb:PALB2
gptkb:FTO
gptkb:MYH11
gptkb:NOD2
gptkb:PKD1
gptkb:SLC12A3
gptkb:WWOX
gptkb:CYLD
TAT
ABCC6
SALL1
TUBB3
ZNF423
|
|
gptkbp:Entrez_Gene_ID
|
ENSCHR016
|
|
gptkbp:GenBank_accession
|
CM000678
|
|
https://www.w3.org/2000/01/rdf-schema#label
|
chromosome 16 (human)
|
|
gptkbp:karyotype_location
|
16
|
|
gptkbp:number_of_base_pairs
|
90,354,753
|
|
gptkbp:number_of_genes_(approximate)
|
900
|
|
gptkbp:OMIM_entry
|
#613376
|
|
gptkbp:organism
|
gptkb:Homo_sapiens
|
|
gptkbp:partOf
|
human genome
|
|
gptkbp:pattern
|
distinctive
|
|
gptkbp:RefSeq
|
NC_000016.10
|
|
gptkbp:region
|
gptkb:16p12.2
gptkb:16q24.3
gptkb:16q12.1
gptkb:16p11.2
16p13.3
16q22.1
16q24.1
16p13.11
16q23.1
16q13
16q21
|
|
gptkbp:bfsParent
|
gptkb:alpha_globin
|
|
gptkbp:bfsLayer
|
6
|