Statements (53)
| Predicate | Object |
|---|---|
| gptkbp:instanceOf |
chromosomal band
|
| gptkbp:associatedWith |
gptkb:autism_spectrum_disorder
gptkb:Williams_syndrome leukemia deafness Ehlers-Danlos syndrome cystic fibrosis osteogenesis imperfecta |
| gptkbp:band |
gptkb:7q34
7q21.3 7q32.1 7q22.1 7q31.2 7p15.3 7q21.11 7p13 7p14.1 7p21.1 7p22.1 7q11.21 7q11.23 7q31.1 7q36.3 |
| gptkbp:centromerePosition |
metacentric
|
| gptkbp:containsGene |
gptkb:EGFR
gptkb:PMS2 gptkb:ELN gptkb:FOXP2 gptkb:GHR gptkb:CFTR gptkb:BRAF gptkb:MET gptkb:AUTS2 gptkb:COL1A2 gptkb:GLI3 gptkb:GRM3 gptkb:IKZF1 gptkb:TWIST1 |
| gptkbp:Entrez_Gene_ID |
gptkb:ENSG00000157764
|
| gptkbp:foundIn |
gptkb:Mus_musculus
gptkb:Homo_sapiens |
| https://www.w3.org/2000/01/rdf-schema#label |
chromosome 7
|
| gptkbp:karyotypeLocation |
7p
7q |
| gptkbp:length |
about 159 million base pairs
|
| gptkbp:numberOfGenes |
over 1,000
|
| gptkbp:OMIMEntry |
#612411
|
| gptkbp:percentageOfHumanGenome |
about 5.5%
|
| gptkbp:RefSeq |
gptkb:NC_000007.14
|
| gptkbp:bfsParent |
gptkb:HGF
gptkb:BRAF gptkb:PIK3CG |
| gptkbp:bfsLayer |
5
|