chromosome 8 (human)

GPTKB entity

Statements (146)
Predicate Object
gptkbp:instanceOf chromosomal band
gptkbp:associatedWith gptkb:Burkitt_lymphoma
gptkb:Charcot-Marie-Tooth_disease
gptkb:Williams_syndrome
Cohen syndrome
Congenital hypothyroidism
Hereditary sensory neuropathy type I
Langer-Giedion syndrome
Lissencephaly
Trichorhinophalangeal syndrome
gptkbp:bandingPattern gptkb:G-banding
gptkbp:centromerePosition submetacentric
gptkbp:containsGene gptkb:BLK
gptkb:FGFR1
gptkb:NBN
gptkb:WRN
gptkb:LPL
gptkb:GATA4
gptkb:NAT1
gptkb:SLC39A1
gptkb:MYC
gptkb:TUSC3
gptkb:SLC20A2
PPP2R2A
KCNK9
CSMD1
EXT1
MSRA
MTUS1
NAT2
NATP
PCM1
PLAG1
SLC39A10
SLC39A100
SLC39A11
SLC39A12
SLC39A13
SLC39A14
SLC39A15
SLC39A16
SLC39A17
SLC39A18
SLC39A19
SLC39A2
SLC39A20
SLC39A21
SLC39A22
SLC39A23
SLC39A24
SLC39A25
SLC39A26
SLC39A27
SLC39A28
SLC39A29
SLC39A3
SLC39A30
SLC39A31
SLC39A32
SLC39A33
SLC39A34
SLC39A35
SLC39A36
SLC39A37
SLC39A38
SLC39A39
SLC39A4
SLC39A40
SLC39A41
SLC39A42
SLC39A43
SLC39A44
SLC39A45
SLC39A46
SLC39A47
SLC39A48
SLC39A49
SLC39A5
SLC39A50
SLC39A51
SLC39A52
SLC39A53
SLC39A54
SLC39A55
SLC39A56
SLC39A57
SLC39A58
SLC39A59
SLC39A6
SLC39A60
SLC39A61
SLC39A62
SLC39A63
SLC39A64
SLC39A65
SLC39A66
SLC39A67
SLC39A68
SLC39A69
SLC39A7
SLC39A70
SLC39A71
SLC39A72
SLC39A73
SLC39A74
SLC39A75
SLC39A76
SLC39A77
SLC39A78
SLC39A79
SLC39A8
SLC39A80
SLC39A81
SLC39A82
SLC39A83
SLC39A84
SLC39A85
SLC39A86
SLC39A87
SLC39A88
SLC39A89
SLC39A90
SLC39A91
SLC39A92
SLC39A93
SLC39A94
SLC39A95
SLC39A96
SLC39A97
SLC39A98
SLC39A99
SLC45A4
TRPS1
gptkbp:discoveredBy human geneticists
https://www.w3.org/2000/01/rdf-schema#label chromosome 8 (human)
gptkbp:karyotype 46,XX or 46,XY
gptkbp:length ~146 million base pairs
gptkbp:locatedOnChromosome 8
gptkbp:location gptkb:nucleus
gptkbp:numberOfGenes ~800
gptkbp:numberOfPairs ~146,364,022
gptkbp:organism gptkb:Homo_sapiens
gptkbp:partOf human genome
gptkbp:referenceGenome gptkb:GRCh38.p14
gptkbp:bfsParent gptkb:Myc
gptkbp:bfsLayer 6