Literature summary for 2.7.10.1 extracted from

Tartaglia, M.; Valeri, S.; Velardi, F.; Di Rocco, C.; Battaglia, P.A.
Trp290Cys mutation in exon IIIa of the fibroblast growth factor receptor 2 (FGFR2) gene is associated with Pfeiffer syndrome (1997), Hum. Genet., 99, 602-606.

Protein Variants

Protein Variants	Comment	Organism
additional information	Trp290Cys mutation in exon IIIa of the fibroblast growth factor receptor 2 gene is associated with Pfeiffer syndrome	Homo sapiens

Organism	UniProt	Comment	Textmining
Homo sapiens	P21802	-	-

Synonyms	Comment	Organism
fibroblast growth factor receptor 2	-	Homo sapiens

Use of this online version of BRENDA is free under the CC BY 4.0 license. See terms of use for full details.

Release 2023.1 (January 2023)