Statements (33)
| Predicate | Object |
|---|---|
| gptkbp:instanceOf |
gptkb:gene
|
| gptkbp:alias |
gptkb:SCC1
hHR21 NXP1 |
| gptkbp:associatedWith |
gptkb:Cornelia_de_Lange_syndrome
cohesinopathies |
| gptkbp:discoveredIn |
1997
|
| gptkbp:encodes |
gptkb:RAD21_protein
|
| gptkbp:Entrez_Gene_ID |
gptkb:ENSG00000164754
5885 |
| gptkbp:expressedIn |
various tissues
|
| gptkbp:foundIn |
gptkb:Homo_sapiens
|
| gptkbp:function |
DNA repair
regulation of gene expression sister chromatid cohesion |
| gptkbp:HGNC_ID |
gptkb:HGNC:9817
|
| gptkbp:interactsWith |
gptkb:SMC1A_protein
gptkb:SMC3_protein gptkb:STAG2_protein |
| gptkbp:involvedIn |
gptkb:cohesin_complex
|
| gptkbp:locatedOnChromosome |
gptkb:8q24.11
chromosome 8 |
| gptkbp:mutationAssociatedWith |
developmental disorders
cancer susceptibility |
| gptkbp:orthologIn |
gptkb:Mus_musculus
gptkb:Drosophila_melanogaster |
| gptkbp:proteinFamily |
kleisin family
|
| gptkbp:regulates |
cell cycle progression
chromosome segregation |
| gptkbp:UniProtID |
gptkb:O60216
|
| gptkbp:bfsParent |
gptkb:SCC1_homolog
|
| gptkbp:bfsLayer |
7
|
| https://www.w3.org/2000/01/rdf-schema#label |
RAD21 gene
|