Literature summary for 2.7.10.1 extracted from

Tavormina, P.L.; Rimoin, D.L.; Cohn, D.H.; Zhu, Y.Z.; Shiang, R.; Wasmuth, J.J.
Another mutation that results in the substitution of an unpaired cysteine residue in the extracellular domain of FGFR3 in thanatophoric dysplasia type I (1995), Hum. Mol. Genet., 4, 2175-2177.

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Protein Variants

Protein Variants	Comment	Organism
additional information	mutation that results in the substitution of an unpaired cysteine residue in the extracellular domain of FGFR3 in thanatophoric dysplasia type I	Homo sapiens

Organism

Organism	UniProt	Comment	Textmining
Homo sapiens	P22607	-	-

Synonyms

Synonyms	Comment	Organism
fibroblast growth factor receptor 3	-	Homo sapiens

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Release 2023.1 (January 2023)