|
gptkbp:instanceOf
|
gptkb:chromosomal_band
|
|
gptkbp:compatibleWith
|
females
most females
|
|
gptkbp:contains
|
pseudoautosomal regions
euchromatin
heterochromatin
|
|
gptkbp:containsGene
|
gptkb:SRY
gptkb:AMELY
gptkb:TSPY
gptkb:ZFY
DAZ1
|
|
gptkbp:discoveredBy
|
gptkb:Nettie_Stevens
|
|
gptkbp:discoveredIn
|
1905
|
|
gptkbp:doesNotRecombineWith
|
chromosome X (except pseudoautosomal regions)
|
|
gptkbp:Entrez_Gene_ID
|
ENSG00000129873
|
|
gptkbp:foundIn
|
gptkb:Homo_sapiens
mammals
|
|
gptkbp:haploidIn
|
males
|
|
gptkbp:hasAluElements
|
yes
|
|
gptkbp:hasCentromere
|
yes
|
|
gptkbp:hasCentromericRegion
|
yes
|
|
gptkbp:hasHaplogroups
|
yes
|
|
gptkbp:hasLongArm
|
yes
|
|
gptkbp:hasNonRecombiningRegion
|
yes
|
|
gptkbp:hasPalindromicSequences
|
yes
|
|
gptkbp:hasPseudoautosomalRegion
|
yes
|
|
gptkbp:hasSatelliteDNA
|
yes
|
|
gptkbp:hasShortArm
|
yes
|
|
gptkbp:hasTelomere
|
yes
|
|
gptkbp:inheritsFrom
|
father
|
|
gptkbp:involvedIn
|
sex determination
|
|
gptkbp:isAutosome
|
no
|
|
gptkbp:isSexChromosome
|
yes
|
|
gptkbp:isSmallestHumanChromosome
|
yes
|
|
gptkbp:karyotypeDesignation
|
46,XY (in humans)
|
|
gptkbp:length
|
~57 million base pairs
|
|
gptkbp:mutationAssociatedWith
|
gptkb:Swyer_syndrome
male infertility
Turner syndrome (if missing)
|
|
gptkbp:numberOfGenes
|
~70
|
|
gptkbp:OMIM
|
400000
|
|
gptkbp:orthologIn
|
gptkb:chromosome_X
|
|
gptkbp:presentIn
|
males
|
|
gptkbp:RefSeq
|
NC_000024.10
|
|
gptkbp:sexChromosome
|
gptkb:male
|
|
gptkbp:symbol
|
Y
|
|
gptkbp:usedIn
|
forensic science
genetic genealogy
paternal lineage tracing
|
|
gptkbp:bfsParent
|
gptkb:GRCh37
|
|
gptkbp:bfsLayer
|
7
|
|
https://www.w3.org/2000/01/rdf-schema#label
|
chromosome Y
|