Annotation Detail
Information
- Associated Genes
- FGFR2
- Associated Variants
-
FGFR2 c.1087+1304G>A
(
ENST00000357555.9,
ENST00000683211.1,
ENST00000369061.8,
ENST00000346997.6,
ENST00000682772.1,
ENST00000457416.7,
ENST00000684153.1,
ENST00000356226.8,
ENST00000478859.5,
ENST00000613048.4,
ENST00000682550.1,
ENST00000638709.2,
ENST00000369056.5,
ENST00000360144.7,
ENST00000358487.10,
ENST00000369060.8,
ENST00000351936.11,
ENST00000369059.5 )
FGFR2 c.1087+1304G>A ( ENST00000346997.6, ENST00000351936.11, ENST00000356226.8, ENST00000357555.9, ENST00000358487.10, ENST00000360144.7, ENST00000369056.5, ENST00000369059.5, ENST00000369060.8, ENST00000369061.8, ENST00000457416.7, ENST00000478859.5, ENST00000613048.4, ENST00000638709.2, ENST00000682550.1, ENST00000682772.1, ENST00000683211.1, ENST00000684153.1 ) - Associated Disease
- Craniofacial dysostosis type 1
- Source Database
- DisGeNET
- Description
- Skulls of Fgfr2(C342Y/+) mice differ from normal littermates in a comparable manner with differences between the skulls of humans with Crouzon syndrome and those of unaffected individuals.
- Pubmed
- 17105336
- Original source reporting the Gene Disease association
- BeFree
- DisGENET score for the Gene Disease association
- 0.332486326115694
- Year of publication
- 2006
Drugs