| Health / Medical Topics |
FGFR3 Gene
This gene plays a role in bone development and maintenance and mutations in the gene are associated with craniosynostosis and several types of skeletal dysplasia. (NCI Thesaurus)
YOU MAY ALSO LIKE
Human FGFR2 wild-type allele is located within 10q26 and is approximately 875 kb in length. This allele, which encodes fibroblast growth factor…
A variation in the amino acid sequence for the fibroblast growth factor receptor 2 protein.
A change in the nucleotide sequence of the FGFR2 gene.
This gene plays a role in mitogenesis and differentiation and mutations in the gene are associated with craniosynostotic syndromes and bone…
A fusion protein (526 aa, ~60 kDa) encoded by the FGFR1OP2/FGFR1 fusion gene. This protein is comprised of the first 2 coiled-coil…
A fusion gene that results from a chromosomal insertion ins(12;8)(p11;p11p22) that fuses exon 4 of the FGFR1OP2 gene with exon 9 of…
