gptkbp:instanceOf
|
gptkb:gene
|
gptkbp:alternativeName
|
gptkb:GAP
gptkb:RasGAP
gptkb:p120-RasGAP
|
gptkbp:associatedWith
|
gptkb:Parkes_Weber_syndrome
gptkb:capillary_malformation-arteriovenous_malformation_syndrome
|
gptkbp:discoveredBy
|
gptkb:Kazusa_DNA_Research_Institute
|
gptkbp:domain
|
gptkb:PH_domain
C2 domain
SH2 domain
SH3 domain
|
gptkbp:encodes
|
gptkb:RAS_p21_protein_activator_1
|
gptkbp:Entrez_Gene_ID
|
gptkb:ENSG00000145715
5921
|
gptkbp:expressedIn
|
various tissues
|
gptkbp:firstDescribed
|
1992
|
gptkbp:function
|
gptkb:GTPase-activating_protein_for_RAS
|
gptkbp:HGNC_ID
|
9871
|
https://www.w3.org/2000/01/rdf-schema#label
|
RASA1
|
gptkbp:interactsWith
|
gptkb:RAS_proteins
phospholipids
|
gptkbp:length
|
1047 amino acids
|
gptkbp:locatedOnChromosome
|
5q14.3
|
gptkbp:molecularWeight
|
120 kDa
|
gptkbp:mutationAssociatedWith
|
vascular anomalies
|
gptkbp:OMIM
|
139150
|
gptkbp:orthologInMouse
|
gptkb:Rasa1
|
gptkbp:regulates
|
gptkb:RAS/MAPK_signaling_pathway
|
gptkbp:subcellularLocation
|
gptkb:cytoplasm
gptkb:plasma_membrane
|
gptkbp:UniProtID
|
gptkb:P20936
|
gptkbp:bfsParent
|
gptkb:HRAS1
gptkb:P01116
gptkb:RASH_HUMAN
gptkb:human_HRAS
gptkb:3265_(HRAS)
gptkb:KEGG:_hsa04014
gptkb:P01112_(HRAS)
|
gptkbp:bfsLayer
|
6
|