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FgfR2IIIa-F, FgfR2IIITM-R Primer Detail
Primers
  • Name
    FgfR2IIIa-F, FgfR2IIITM-R
  • Primer 1 Sequence
    CCCATCCTCCAAGCTGGACTGCCT
  • Primer 2 Sequence
    GCTTGGTCAGCTTGTGCACAGCTGG
  • ID
    MGI:7284759
  • Region Covered
    exon 7-10
Genes
Fgfr2 fibroblast growth factor receptor 2
Expression
  • Assay Results
    4
References
J:72517 Hajihosseini MK, et al., A splicing switch and gain-of-function mutation in FgfR2-IIIc hemizygotes causes Apert/Pfeiffer-syndrome-like phenotypes. Proc Natl Acad Sci U S A. 2001 Mar 27;98(7):3855-60
Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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Send questions and comments to User Support. 		last database update
03/25/2025
MGI 6.24 		The Jackson Laboratory