|
gptkbp:instanceOf
|
chromosomal band
|
|
gptkbp:associatedWith
|
gptkb:Alport_syndrome
gptkb:Charcot-Marie-Tooth_disease
gptkb:Glioblastoma
gptkb:Hereditary_hemorrhagic_telangiectasia
gptkb:Medullary_thyroid_carcinoma
gptkb:Multiple_endocrine_neoplasia_type_2
gptkb:Waardenburg_syndrome
gptkb:Cowden_syndrome
Congenital nephrotic syndrome
|
|
gptkbp:autosome
|
true
|
|
gptkbp:bandingPattern
|
gptkb:G-banding
|
|
gptkbp:centromerePosition
|
submetacentric
|
|
gptkbp:containsGene
|
gptkb:CYP2C9
gptkb:CYP2C19
gptkb:GATA3
gptkb:ADAM12
gptkb:C10orf2
gptkb:C10orf67
gptkb:C10orf88
gptkb:C10orf90
gptkb:LRRTM3
gptkb:NEBL
gptkb:PAX2
gptkb:PRKG1
gptkb:RET
gptkb:VIM
gptkb:PTEN
gptkb:EGR2
gptkb:FGFR2
gptkb:GLUD1
KCNMA1
C10orf105
C10orf118
C10orf131
C10orf142
C10orf143
C10orf54
C10orf62
C10orf71
C10orf72
C10orf82
C10orf99
|
|
gptkbp:Entrez_Gene_ID
|
10
|
|
gptkbp:foundIn
|
gptkb:Homo_sapiens
|
|
https://www.w3.org/2000/01/rdf-schema#label
|
human chromosome 10
|
|
gptkbp:karyotypeDesignation
|
10
|
|
gptkbp:length
|
133,797,422 base pairs
|
|
gptkbp:numberOfGenes
|
800-900
|
|
gptkbp:numberOfPairs
|
133,797,422
|
|
gptkbp:RefSeq
|
NC_000010.11
|
|
gptkbp:bfsParent
|
gptkb:Nodal_gene
|
|
gptkbp:bfsLayer
|
7
|