|
gptkbp:instanceOf
|
chromosomal band
|
|
gptkbp:arms
|
q
p
|
|
gptkbp:associatedWith
|
schizophrenia
type 1 diabetes
autoimmune diseases
psoriasis
hereditary hemochromatosis
|
|
gptkbp:bandingPattern
|
distinct G-banding pattern
|
|
gptkbp:centromerePosition
|
metacentric
|
|
gptkbp:contains
|
gptkb:PARK2_gene
gptkb:HLA_genes
gptkb:major_histocompatibility_complex
gptkb:COL11A2_gene
gptkb:NOTCH4_gene
gptkb:TNF_gene
gptkb:GLO1_gene
gptkb:HFE_gene
gptkb:PRDM1_gene
gptkb:RUNX2_gene
gptkb:VEGF_gene
gptkb:C4A_gene
gptkb:C4B_gene
HIST1H1A gene
HIST1H2AA gene
HIST1H2BA gene
HIST1H3A gene
HIST1H4A gene
|
|
gptkbp:Entrez_Gene_ID
|
6
|
|
gptkbp:foundIn
|
gptkb:Homo_sapiens
|
|
https://www.w3.org/2000/01/rdf-schema#label
|
human chromosome 6
|
|
gptkbp:karyotypeDesignation
|
46,XX or 46,XY
|
|
gptkbp:location
|
between chromosome 5 and chromosome 7
|
|
gptkbp:numberOfCopyPerCell
|
2
|
|
gptkbp:numberOfGenes
|
over 2000
|
|
gptkbp:numberOfPairs
|
170805979
|
|
gptkbp:RefSeq
|
NC_000006.12
|
|
gptkbp:bfsParent
|
gptkb:CMH9
gptkb:SLC9C26
gptkb:SLC9C56
gptkb:TIS8
|
|
gptkbp:bfsLayer
|
7
|