|
gptkbp:instanceOf
|
gptkb:protein
gptkb:gene
|
|
gptkbp:alsoKnownAs
|
gptkb:SCF
gptkb:mast_cell_growth_factor
gptkb:steel_factor
gptkb:stem_cell_factor
|
|
gptkbp:associatedWith
|
gptkb:anemia
infertility
pigmentation disorders
|
|
gptkbp:binds
|
c-KIT receptor
|
|
gptkbp:biologicalProcess
|
cell differentiation
cell proliferation
cell survival
growth factor activity
|
|
gptkbp:category
|
cytokine
|
|
gptkbp:cellularComponent
|
gptkb:cell_membrane
extracellular region
|
|
gptkbp:discoveredBy
|
T. N. C. Wells
|
|
gptkbp:discoveredIn
|
1990
|
|
gptkbp:encodedBy
|
gptkb:KITLG_gene
|
|
gptkbp:Entrez_Gene_ID
|
4254
|
|
gptkbp:expressedIn
|
gptkb:skin
gptkb:placenta
gptkb:testis
bone marrow
fetal liver
|
|
gptkbp:foundIn
|
gptkb:Mus_musculus
gptkb:Homo_sapiens
|
|
gptkbp:function
|
melanogenesis
hematopoiesis
gametogenesis
|
|
gptkbp:gene
|
gptkb:KITLG
|
|
https://www.w3.org/2000/01/rdf-schema#label
|
KIT ligand
|
|
gptkbp:locatedOnChromosome
|
chromosome 12q22 (human)
|
|
gptkbp:mutationAssociatedWith
|
gptkb:piebaldism
congenital deafness
germ cell loss
|
|
gptkbp:OMIM
|
184745
|
|
gptkbp:orthologIn
|
gptkb:mouse
gptkb:zebrafish
right
|
|
gptkbp:postTranslationalModification
|
cleavage
glycosylation
|
|
gptkbp:recipient
|
KIT (CD117)
|
|
gptkbp:regulates
|
mast cell development
melanocyte migration
primordial germ cell survival
|
|
gptkbp:structure
|
homodimer
|
|
gptkbp:UniProtID
|
P21583
|
|
gptkbp:bfsParent
|
gptkb:Stem_Cell_Factor
|
|
gptkbp:bfsLayer
|
7
|