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
|