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RUNX2 binds CBFB
RUNX2 binds CBFB
Item
http://www.wikidata.org/entity/Q50290666
Q50290666
about
Transcriptional regulation by RUNX2
P527
Q45316819-B9CF44C2-57DB-4E77-88B7-5832609AD6CB
P527
RUNX2 binds CBFB
Item
http://www.wikidata.org/entity/Q50290666
description
An instance of the biological reaction RUNX2 binds CBFB in Homo sapiens
@en
biologisch proces
@nl
name
RUNX2 binds CBFB
@en
type
Item
label
RUNX2 binds CBFB
@en
prefLabel
RUNX2 binds CBFB
@en
P2860
Q50290666-1B573EBA-C316-4192-8A33-80D9E2C8CE99
Q50290666-4A9E748C-5A56-4120-B0E6-CD6921338E4E
Q50290666-B91E4E78-BCAC-47E5-9659-15DE7C8F7D97
Q50290666-BA14C900-0E8E-41AB-98E6-59EF9EA43EB4
Q50290666-C7037695-6C5F-4F0E-AFCD-B954059C2FF3
Q50290666-EF75D4D4-A44C-4008-BE82-06E025987589
P2888
Q50290666-AEAE7F68-7FA1-4490-B8EE-910F9F1525B6
P31
Q50290666-C95C736A-1750-416D-93EE-7F0D3B4154CC
P361
Q50290666-ADB07E38-9139-4E5E-AFDB-50E70AD065D4
P3937
Q50290666-9043F53F-943A-4963-8ED6-AD64A80A9385
P527
Q50290666-03AE62E2-E7CD-45E4-BDB1-58495C7C463C
Q50290666-880F9994-6085-475F-B15C-C53A70396CC5
Q50290666-A6828CF4-CA58-4E53-BDA5-50233964474C
P703
Q50290666-153869AE-563A-4054-AC8C-12B8CDAD2ADC
P2860
Cbfa1, a candidate gene for cleidocranial dysplasia syndrome, is essential for osteoblast differentiation and bone development
Mutations in the RUNX2 gene in patients with cleidocranial dysplasia
Cbfbeta interacts with Runx2 and has a critical role in bone development
Cbfβ deletion in mice recapitulates cleidocranial dysplasia and reveals multiple functions of Cbfβ required for skeletal development.
Core-binding factor beta interacts with Runx2 and is required for skeletal development.
Missense mutations abolishing DNA binding of the osteoblast-specific transcription factor OSF2/CBFA1 in cleidocranial dysplasia.
P2888
reactome:R-HSA-8865425
P31
biological process
P361
Transcriptional regulation by RUNX2
P3937
R-HSA-8865425
http://www.w3.org/2001/XMLSchema#string
P527
Core-binding factor subunit beta
RUNX2
RUNX2:CBFB
P703
Homo sapiens