Statements (32)
| Predicate | Object |
|---|---|
| gptkbp:instanceOf |
chromosomal band
|
| gptkbp:arms |
q arm
p arm |
| gptkbp:associatedWith |
type 1 diabetes
autoimmune diseases psoriasis narcolepsy celiac disease hereditary hemochromatosis |
| gptkbp:centromere_position |
submetacentric
|
| gptkbp:contains |
gptkb:PARK2_gene
gptkb:major_histocompatibility_complex_(MHC) gptkb:HLA_genes gptkb:TNF_gene gptkb:CYP21A2_gene gptkb:GLO1_gene gptkb:HFE_gene gptkb:PRDM1_gene gptkb:RUNX2_gene gptkb:VEGF_gene |
| gptkbp:Entrez_Gene_ID |
6
|
| https://www.w3.org/2000/01/rdf-schema#label |
chromosome 6 (human)
|
| gptkbp:karyotype_location |
6
|
| gptkbp:length_(Mb) |
~171
|
| gptkbp:number_of_base_pairs |
~170,805,979
|
| gptkbp:number_of_genes_(approximate) |
1,557
|
| gptkbp:organism |
gptkb:Homo_sapiens
|
| gptkbp:partOf |
human genome
|
| gptkbp:pattern |
distinctive G-banding
|
| gptkbp:RefSeq |
NC_000006.12
|
| gptkbp:bfsParent |
gptkb:major_histocompatibility_complex_(MHC)
|
| gptkbp:bfsLayer |
6
|