Annotation Detail
Information
- Associated Genes
- FGFR1
- Associated Variants
-
FGFR1 MUTATION
FGFR1 MUTATION - Associated Disease
- cleidocranial dysplasia
- Source Database
- DisGeNET
- Description
- Expression of RUNX2 and its signaling partners TCF7, FGFR1/2 in cleidocranial dysplasia.
- Pubmed
- 25738174
- Section of the abstract supporting the evidence
- TITLE
- Number of the section of the abstract supporting the evidence
- 0
- Number of the sentence supporting the evidence
- 0
- Original source reporting the Gene Disease association
- BeFree
- DisGENET score for the Gene Disease association
- 0.000271441872080303
Drugs