|
gptkbp:instanceOf
|
gptkb:chromosomal_band
|
|
gptkbp:associatedWith
|
gptkb:cancer
gptkb:retinoblastoma
gptkb:Hirschsprung_disease
prostate cancer
13q deletion syndrome
|
|
gptkbp:centromere_position
|
acrocentric
|
|
gptkbp:chromosome_type
|
autosome
|
|
gptkbp:containsGene
|
gptkb:DLEU1
gptkb:DLEU2
gptkb:PCDH9
gptkb:RB1
gptkb:SLC15A1
gptkb:SLC7A1
gptkb:BRCA2
gptkb:COL4A1
gptkb:FLT1
gptkb:SOX21
gptkb:EDNRB
TNFSF11
MIPEP
GPC5
GPC6
STARD13
ZIC2
|
|
gptkbp:Entrez_Gene_ID
|
gptkb:ENSG00000139618
|
|
gptkbp:karyotype_location
|
13q
|
|
gptkbp:number_of_base_pairs
|
~114 million
|
|
gptkbp:number_of_chromosomes_in_human
|
23 pairs
|
|
gptkbp:numberOfGenes
|
~300 to 400
|
|
gptkbp:organism
|
gptkb:Homo_sapiens
|
|
gptkbp:partOf
|
human genome
|
|
gptkbp:pattern
|
gptkb:G-banding
|
|
gptkbp:RefSeq
|
NC_000013.11
|
|
gptkbp:region
|
gptkb:13q12
gptkb:13q14
gptkb:13q34
gptkb:13q14.3
13q14.2
13q31.1
13q22
13q32.1
13p11
13q21
13q21.1
13q31
13q32
13q33
|
|
gptkbp:bfsParent
|
gptkb:ParaHox_genes
gptkb:CDC16
|
|
gptkbp:bfsLayer
|
8
|
|
https://www.w3.org/2000/01/rdf-schema#label
|
chromosome 13 (human)
|