gptkbp:instanceOf
|
gptkb:protein
|
gptkbp:alternativeName
|
NTRKR2
Neurotrophic tyrosine kinase, receptor-related 2
|
gptkbp:associatedWith
|
gptkb:Robinow_syndrome
brachydactyly type B1
|
gptkbp:cellularComponent
|
gptkb:plasma_membrane
|
gptkbp:discoveredBy
|
1992
|
gptkbp:domain
|
immunoglobulin-like domain
tyrosine kinase domain
frizzled-like cysteine-rich domain
|
gptkbp:encodedBy
|
ROR2 gene
|
gptkbp:Entrez_Gene_ID
|
ENSG00000185483
|
gptkbp:expressedIn
|
embryonic tissues
mesenchymal cells
|
gptkbp:fullName
|
Receptor tyrosine kinase-like orphan receptor 2
|
gptkbp:function
|
gptkb:receptor_tyrosine_kinase
gptkb:Wnt_signaling_pathway
|
gptkbp:gene
|
gptkb:ROR2
|
gptkbp:HGNC_ID
|
10255
|
https://www.w3.org/2000/01/rdf-schema#label
|
ROR2
|
gptkbp:interactsWith
|
gptkb:Frizzled_receptors
gptkb:WNT5A
|
gptkbp:locatedOnChromosome
|
gptkb:chromosome_9
|
gptkbp:location
|
9q22.31
|
gptkbp:molecularWeight
|
104 kDa
|
gptkbp:mutationAssociatedWith
|
skeletal dysplasia
|
gptkbp:OMIM
|
602337
|
gptkbp:organism
|
gptkb:Homo_sapiens
|
gptkbp:PDB
|
5FZC
|
gptkbp:RefSeq
|
NM_004560
|
gptkbp:UniProtID
|
Q01974
|
gptkbp:bfsParent
|
gptkb:Wnt-5a
gptkb:Wnt5a
|
gptkbp:bfsLayer
|
8
|