Statements (30)
| Predicate | Object |
|---|---|
| gptkbp:instanceOf |
chromosomal band
|
| gptkbp:arms |
p and q
|
| gptkbp:associatedWith |
gptkb:Marfan_syndrome
gptkb:Angelman_syndrome gptkb:Oculocutaneous_albinism_type_2 gptkb:Prader-Willi_syndrome |
| gptkbp:autosome |
true
|
| gptkbp:centromerePosition |
submetacentric
|
| gptkbp:containsGene |
gptkb:CYFIP1
gptkb:FBN1 gptkb:GABRB3 gptkb:HERC2 gptkb:OCA2 gptkb:UBE3A |
| gptkbp:containsImprintedRegion |
gptkb:15q11-q13
|
| gptkbp:Entrez_Gene_ID |
15
|
| gptkbp:foundIn |
gptkb:Mus_musculus
gptkb:Homo_sapiens |
| https://www.w3.org/2000/01/rdf-schema#label |
chromosome 15
|
| gptkbp:inHumanGenome |
true
|
| gptkbp:karyotypeLocation |
gptkb:15q11-q13
|
| gptkbp:length |
~101 million base pairs
|
| gptkbp:locatedOnChromosome |
15
|
| gptkbp:numberOfGenes |
~600
|
| gptkbp:numberOfPairs |
~101,991,189
|
| gptkbp:OMIM |
#601626
|
| gptkbp:RefSeq |
NC_000015.10
|
| gptkbp:bfsParent |
gptkb:CYP1A2
gptkb:Hist |
| gptkbp:bfsLayer |
5
|