Annotation Detail
Information
- Associated Genes
- F2R
- Associated Variants
-
F2R MUTATION
F2R MUTATION - Associated Disease
- OVERLAP CONNECTIVE TISSUE DISEASE
- Source Database
- DisGeNET
- Description
- Thrombin receptor deficiency leads to a high bone mass phenotype by decreasing the RANKL/OPG ratio.
- Pubmed
- 25460576
- 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