gptkbp:instanceOf
|
gptkb:protein
gptkb:gene
|
gptkbp:alternativeName
|
Pasha
|
gptkbp:associatedWith
|
gptkb:22q11.2_deletion_syndrome
|
gptkbp:biologicalProcess
|
double-stranded RNA binding
miRNA processing
|
gptkbp:chromosomeArm
|
gptkb:22q11.21
|
gptkbp:component
|
gptkb:Microprocessor_complex
|
gptkbp:discoveredIn
|
2004
|
gptkbp:encodes
|
gptkb:Microprocessor_complex_subunit_DGCR8
|
gptkbp:Entrez_Gene_ID
|
ENSG00000163682
54487
|
gptkbp:expressedIn
|
gptkb:nucleus
|
gptkbp:fullName
|
gptkb:DiGeorge_syndrome_critical_region_gene_8
|
gptkbp:function
|
RNA-binding protein
microRNA biogenesis
|
gptkbp:geneType
|
protein-coding
|
gptkbp:GOID
|
GO:0035196
|
https://www.w3.org/2000/01/rdf-schema#label
|
DGCR8
|
gptkbp:interactsWith
|
gptkb:DROSHA
|
gptkbp:locatedOnChromosome
|
chromosome 22
|
gptkbp:mutationAssociatedWith
|
gptkb:DiGeorge_syndrome
|
gptkbp:OMIM
|
609527
|
gptkbp:organism
|
gptkb:Homo_sapiens
|
gptkbp:orthologIn
|
gptkb:Danio_rerio
gptkb:Mus_musculus
gptkb:Drosophila_melanogaster
|
gptkbp:subcellularLocation
|
gptkb:nucleus
|
gptkbp:UniProtID
|
Q8WYQ5
|
gptkbp:bfsParent
|
gptkb:ERH
|
gptkbp:bfsLayer
|
6
|