fibroblast growth factor 10; FGF-10; keratinocyte growth factor 2 (FGF10)
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Function
- role in the regulation of embryonic development, cell proliferation & cell differentiation
- required for normal branching morphogenesis
- may play a role in wound healing
- interacts with FGFR1 & FGFR2
- interacts with FGFBP1
Structure
- belongs to the heparin-binding growth factors family
Compartment
Pathology
- defects in FGF10 are the cause of autosomal dominant aplasia of lacrimal & salivary glands
- defects in FGF10 are a cause of Levy-Hollister syndrome
More general terms
References
- ↑ UniProt http://www.uniprot.org/uniprot/O15520.html
- ↑ NIEHS-SNPs http://egp.gs.washington.edu/data/fgf10/
Database
- Entrez gene: http://www.ncbi.nlm.nih.gov/sites/entrez?db=gene&cmd=Retrieve&dopt=Graphics&list_uids=2255
- Kegg: http://www.genome.jp/dbget-bin/www_bget?hsa:2255
- OMIM: https://mirror.omim.org/entry/149730
- OMIM: https://mirror.omim.org/entry/180920
- OMIM: https://mirror.omim.org/entry/602115
- UniProt: http://www.uniprot.org/uniprot/O15520.html