|
gptkbp:instanceOf
|
chromosomal band
|
|
gptkbp:arms
|
q
p
|
|
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:bandingPattern
|
distinctive G-banding pattern
|
|
gptkbp:centromerePosition
|
metacentric
|
|
gptkbp:containsGene
|
gptkb:TSC2
gptkb:CREBBP
gptkb:MC1R
gptkb:HBA1
gptkb:HBA2
gptkb:CDH1
gptkb:FTO
gptkb:MYH11
gptkb:NOD2
gptkb:PKD1
gptkb:SLC12A3
gptkb:WWOX
gptkb:CYLD
|
|
gptkbp:Entrez_Gene_ID
|
ENSG00000196136
|
|
gptkbp:foundIn
|
gptkb:Homo_sapiens
|
|
gptkbp:homologousPair
|
yes
|
|
https://www.w3.org/2000/01/rdf-schema#label
|
chromosome 16
|
|
gptkbp:karyotypeDesignation
|
46,XX or 46,XY
|
|
gptkbp:length
|
about 90 million base pairs
|
|
gptkbp:location
|
gptkb:nucleus
|
|
gptkbp:numberOfGenes
|
about 900
|
|
gptkbp:numberOfPairs
|
about 90,354,753
|
|
gptkbp:OMIMEntry
|
#613854
|
|
gptkbp:presentIn
|
all human cells except gametes and red blood cells
|
|
gptkbp:RefSeq
|
NC_000016.10
|
|
gptkbp:bfsParent
|
gptkb:FANCA
gptkb:16p11.2
gptkb:mouse_SOD1
gptkb:HBA1_gene
gptkb:HBA2_gene
gptkb:CD19
gptkb:AXIN1
|
|
gptkbp:bfsLayer
|
6
|