| Health / Medical Topics |
FGFR2 Gene
This gene plays a role in mitogenesis and differentiation and mutations in the gene are associated with craniosynostotic syndromes and bone malformations. (NCI Thesaurus)
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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…
Human FGFR1OP2 wild-type allele is located in the vicinity of 12p11.23 and is approximately 28 kb in length. This allele, which encodes…
This gene may be involved in wound responses.
A fusion protein encoded by the FGFR1OP/FGFR1 fusion gene. This protein is comprised of the LIS1 homology domain of the FGFR1 oncogene…
A fusion gene that results from a chromosomal translocation t(6;8)(q27;p11) that fuses exon 5, 6 or 7 of the FGFR1OP gene with…
