Annotation Detail
Information
- Associated Genes
- FGFR2
- Associated Variants
-
FGFR2 c.1087+1300A>C
(
ENST00000369061.8,
ENST00000346997.6,
ENST00000682772.1,
ENST00000357555.9,
ENST00000683211.1,
ENST00000457416.7,
ENST00000356226.8,
ENST00000684153.1,
ENST00000638709.2,
ENST00000478859.5,
ENST00000613048.4,
ENST00000682550.1,
ENST00000360144.7,
ENST00000369059.5,
ENST00000358487.10,
ENST00000369060.8,
ENST00000351936.11,
ENST00000369056.5 )
FGFR3 p.Gly382Arg (p.G382R) ( ENST00000340107.9, ENST00000352904.6, ENST00000412135.7, ENST00000440486.8, ENST00000481110.7 )
FGFR3 p.Gly382Arg (p.G382R) ( ENST00000440486.8, ENST00000340107.9, ENST00000352904.6, ENST00000412135.7, ENST00000481110.7 )
FGFR2 c.1087+1300A>C ( 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 )
FGFR3 p.Gly382Arg (p.G382R) ( ENST00000340107.9, ENST00000352904.6, ENST00000412135.7, ENST00000440486.8, ENST00000481110.7 )
FGFR3 p.Gly382Arg (p.G382R) ( ENST00000340107.9, ENST00000352904.6, ENST00000412135.7, ENST00000440486.8, ENST00000481110.7 ) - Associated Disease
- ACROCEPHALOPOLYSYNDACTYLY TYPE IV
- Source Database
- DisGeNET
- Description
- Gene analysis of these patients showed a T341P mutation in the FGFR2 gene in the patient with Pfeiffer syndrome, and a G380R mutation in the FGFR3 gene in the patient with achondroplasia.
- Pubmed
- 9780920
- Original source reporting the Gene Disease association
- BeFree
- DisGENET score for the Gene Disease association
- 0.00950046552281062
- Year of publication
- 1998
Drugs