|
gptkbp:instanceOf
|
chromosomal band
|
|
gptkbp:bandingPattern
|
distinctive G-banding
|
|
gptkbp:carriesGenesFor
|
gptkb:Duchenne_muscular_dystrophy
gptkb:fragile_X_syndrome
hemophilia
color vision
|
|
gptkbp:contains
|
telomeres
centromere
pseudoautosomal regions
|
|
gptkbp:discoveredBy
|
gptkb:Hermann_Henking
|
|
gptkbp:discoveredIn
|
1890
|
|
gptkbp:Entrez_Gene_ID
|
ENSG000001X
|
|
gptkbp:foundIn
|
humans
mammals
|
|
https://www.w3.org/2000/01/rdf-schema#label
|
X chromosome
|
|
gptkbp:inactivationInFemales
|
gptkb:X-inactivation
|
|
gptkbp:influenced
|
sex determination
|
|
gptkbp:length
|
about 155 million base pairs
|
|
gptkbp:location
|
gptkb:nucleus
|
|
gptkbp:NCBIID
|
gptkb:NC_000023.11
|
|
gptkbp:numberInFemales
|
2
|
|
gptkbp:numberInMales
|
1
|
|
gptkbp:numberOfGenes
|
over 1,000
|
|
gptkbp:OMIM
|
300000
|
|
gptkbp:orthologIn
|
gptkb:Y_chromosome
|
|
gptkbp:partner
|
gptkb:Y_chromosome
|
|
gptkbp:presentIn
|
both males and females
|
|
gptkbp:sexChromosome
|
true
|
|
gptkbp:symbol
|
X
|
|
gptkbp:bfsParent
|
gptkb:CTAG2_gene
gptkb:sex-lethal
gptkb:Xp22.2
gptkb:ARS_(gene)
gptkb:Xq28
gptkb:X_chromosome_(ARAF)
gptkb:Xp21.2
gptkb:dystrophin
gptkb:Angiotensin-converting_enzyme_2
gptkb:angiotensin_I_converting_enzyme_2
|
|
gptkbp:bfsLayer
|
6
|