FGF10 ist ein Gen, das durch das Symbol FGF10 kodiert wird. Andere Namen sind: Fibroblast growth factor 10; FGF-10; Keratinocyte growth factor 2. FGF10 hat eine Masse von 23.44kDa, eine Aminosäurelänge von 208, und ist an folgenden Krankheiten beteiligt: Aplasia of lacrimal and salivary glands; Lacrimo-auriculo-dento-digital syndrome.
Wir bieten 8 FGF10 ELISA-Kits zum qualitativen oder quantitativen Nachweis von FGF10 von Human, Maus und Ratte proben.
Gen- und Proteininformationen
UniProt Zusammenfassung
Plays an important role in the regulation of embryonic development, cell proliferation and cell differentiation. Required for normal branching morphogenesis. May play a role in wound healing.
Entrez Zusammenfassung
The protein encoded by this gene is a member of the fibroblast growth factor (FGF) family. FGF family members possess broad mitogenic and cell survival activities, and are involved in a variety of biological processes, including embryonic development, cell growth, morphogenesis, tissue repair, tumor growth and invasion. This protein exhibits mitogenic activity for keratinizing epidermal cells, but essentially no activity for fibroblasts, which is similar to the biological activity of FGF7. Studies of the mouse homolog of suggested that this gene is required for embryonic epidermal morphogenesis including brain development, lung morphogenesis, and initiation of lim bud formation. This gene is also implicated to be a primary factor in the process of wound healing.
Rolle bei Krankheiten
Aplasia of lacrimal and salivary glands: A rare condition characterized by dry conjunctival mucosae, irritable eyes, epiphora (constant tearing), and xerostomia (dryness of the mouth), which increases risk of dental erosion, dental caries, periodontal disease, and oral infections. ALSG has variable expressivity, and affected individuals may have aplasia or hypoplasia of the lacrimal, parotid, submandibular, and sublingual glands and absence of the lacrimal puncta.
Lacrimo-auriculo-dento-digital syndrome: An autosomal dominant ectodermal dysplasia, a heterogeneous group of disorders due to abnormal development of two or more ectodermal structures. Lacrimo-auriculo-dento-digital syndrome is characterized by aplastic/hypoplastic lacrimal and salivary glands and ducts, cup-shaped ears, hearing loss, hypodontia and enamel hypoplasia, and distal limb segments anomalies. In addition to these cardinal features, facial dysmorphism, malformations of the kidney and respiratory system and abnormal genitalia have been reported. Craniosynostosis and severe syndactyly are not observed.
Sequenzähnlichkeiten
Belongs to the heparin-binding growth factors family.
