|
gptkbp:instanceOf
|
gptkb:chromosomal_band
|
|
gptkbp:associatedWith
|
gptkb:Charcot-Marie-Tooth_disease
gptkb:Waardenburg_syndrome
gptkb:Marfan_syndrome
gptkb:Rett_syndrome
Alström syndrome
Autosomal dominant polycystic kidney disease
Familial hypercholesterolemia
|
|
gptkbp:bandingPattern
|
distinct G-banding pattern
|
|
gptkbp:containsCentromere
|
yes
|
|
gptkbp:containsFusionSite
|
yes
|
|
gptkbp:containsGene
|
gptkb:MSH2
gptkb:ZEB2
gptkb:BCL11A
gptkb:DLX1
gptkb:DLX2
gptkb:LMNA
gptkb:SLC40A1
gptkb:APOB
gptkb:TTN
gptkb:COL3A1
gptkb:PAX3
gptkb:IL1B
MERTK
SLC4A4
ACVR1
MYCN
NFE2L2
ALMS1
GPR75
IL36A
IL36B
IL36G
|
|
gptkbp:containsTelomere
|
yes
|
|
gptkbp:Entrez_Gene_ID
|
gptkb:ENSG00000139618
|
|
gptkbp:foundIn
|
gptkb:Homo_sapiens
|
|
gptkbp:karyotypeLocation
|
2p and 2q arms
|
|
gptkbp:length
|
~242 million base pairs
|
|
gptkbp:locatedOnChromosome
|
2
|
|
gptkbp:numberOfGenes
|
~1300
|
|
gptkbp:origin
|
fusion of two ancestral ape chromosomes
|
|
gptkbp:orthologIn
|
chimpanzee chromosomes 2A and 2B
|
|
gptkbp:RefSeq
|
NC_000002.12
|
|
gptkbp:bfsParent
|
gptkb:SLC9C35
gptkb:SLC9C40
|
|
gptkbp:bfsLayer
|
7
|
|
https://www.w3.org/2000/01/rdf-schema#label
|
human chromosome 2
|