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gptkbp:instanceOf
|
gptkb:chromosomal_band
|
|
gptkbp:associatedWith
|
gptkb:neuroblastoma
gptkb:intellectual_disability
gptkb:1p36_deletion_syndrome
gptkb:cardiomyopathy
congenital heart defects
hearing loss
seizures
developmental delay
|
|
gptkbp:band
|
gptkb:terminal
subtelomeric
distal
|
|
gptkbp:containsGene
|
gptkb:CHD5
gptkb:CAMTA1
gptkb:CASZ1
gptkb:GABRD
gptkb:GNB1
gptkb:HSPG2
gptkb:KCNAB2
gptkb:PEX10
gptkb:PRDM16
gptkb:RERE
gptkb:TP73
gptkb:UBE4B
gptkb:CDC2L1
gptkb:KIF1B
gptkb:MMP23B
SKI
|
|
gptkbp:containsMicroRNA
|
gptkb:miR-34a
gptkb:miR-200a
gptkb:miR-200b
gptkb:miR-429
|
|
gptkbp:genomicCoordinates
|
chr1:0-10,000,000 (approximate)
|
|
gptkbp:isFrequentlyDeletedIn
|
gptkb:neuroblastoma
gptkb:1p36_deletion_syndrome
various cancers
|
|
gptkbp:isTumorSuppressor
|
gptkb:CHD5
gptkb:CAMTA1
gptkb:CASZ1
gptkb:TP73
gptkb:KIF1B
|
|
gptkbp:locatedOn
|
chromosome 1
|
|
gptkbp:locatedOnChromosome
|
gptkb:1p36
|
|
gptkbp:partOf
|
gptkb:short_arm_of_chromosome_1
|
|
gptkbp:bfsParent
|
gptkb:CB2_receptor
gptkb:PINK1
|
|
gptkbp:bfsLayer
|
7
|
|
https://www.w3.org/2000/01/rdf-schema#label
|
chromosome 1p36
|