| Health / Medical Topics |
FGFR3 wt Allele
Human FGFR3 wild-type allele is located in the vicinity of 4p16.3 and is approximately 15 kb in length. This allele, which encodes fibroblast growth factor receptor 3 protein, is involved in mitogenesis, differentiation, and bone development and maintenance. Alterations in the gene resulting in defects cause, achondroplasia, crouzon syndrome, thanatophoric dysplasia, coronal synostosis, hypochondroplasia, bladder and cervix cancers. (NCI Thesaurus)
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