|
gptkbp:instanceOf
|
gptkb:chromosomal_band
|
|
gptkbp:associatedWith
|
gptkb:Ehlers-Danlos_syndrome
gptkb:leukemia
gptkb:autism_spectrum_disorder
gptkb:Williams_syndrome
gptkb:osteogenesis_imperfecta
deafness
cystic fibrosis
|
|
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
|
|
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:RALA
gptkb:LYTIP
gptkb:HGF
gptkb:7q34_(BRAF)
gptkb:BRAF
gptkb:PIK3CG
|
|
gptkbp:bfsLayer
|
6
|
|
https://www.w3.org/2000/01/rdf-schema#label
|
chromosome 7
|