Statements (45)
| Predicate | Object |
|---|---|
| gptkbp:instanceOf |
chromosomal band
|
| gptkbp:associatedWith |
gptkb:congenital_nephrotic_syndrome
gptkb:familial_adenomatous_polyposis gptkb:Edwards_syndrome |
| gptkbp:centromere_position |
submetacentric
|
| gptkbp:chromosome_number |
18
|
| gptkbp:containsGene |
gptkb:TYMS
gptkb:SETBP1 gptkb:DCC gptkb:CDH7 gptkb:GALR1 gptkb:LAMA3 gptkb:MC4R gptkb:SERPINB2 gptkb:TCF4 gptkb:SMAD4 gptkb:BCL2 gptkb:CDH2 gptkb:NEDD4L gptkb:FECH PMAIP1 CABLES1 RBBP8 NETO1 NPC1 SALL3 TSHZ1 YES1 ZADH2 |
| gptkbp:Entrez_Gene_ID |
CHR18
|
| https://www.w3.org/2000/01/rdf-schema#label |
chromosome 18 (human)
|
| gptkbp:location |
gptkb:nucleus
|
| gptkbp:long_arm |
18q
|
| gptkbp:number_of_base_pairs |
approximately 80 million
|
| gptkbp:numberOfGenes |
approximately 261
|
| gptkbp:OMIM |
#113720
|
| gptkbp:organism |
gptkb:Homo_sapiens
|
| gptkbp:partOf |
human genome
|
| gptkbp:pattern |
18p, 18q
|
| gptkbp:RefSeq |
NC_000018.10
|
| gptkbp:short_arm |
18p
|
| gptkbp:type |
autosome
|
| gptkbp:bfsParent |
gptkb:chromosome_18q12.3_(human)
gptkb:myelin_basic_protein |
| gptkbp:bfsLayer |
7
|