Non-annotated gene. Preliminary data : if you are an author who wish to write a full paper/card on this gene, contribute in submission tool
Other Information
Locus ID:
NCBI: 2258
MIM: 300070
HGNC: 3670
Ensembl: ENSG00000129682
Variants:
dbSNP: 2258
ClinVar: 2258
TCGA: ENSG00000129682
COSMIC: FGF13
RNA/Proteins
Expression (GTEx)
Pathways
References
| Pubmed ID | Year | Title | Citations |
|---|---|---|---|
| 38733310 | 2024 | FGF13 enhances the function of TRPV1 by stabilizing microtubules and regulates acute and chronic itch. | 0 |
| 38733310 | 2024 | FGF13 enhances the function of TRPV1 by stabilizing microtubules and regulates acute and chronic itch. | 0 |
| 36988403 | 2023 | The inhibitory role of microRNA-141-3p in human cutaneous melanoma growth and metastasis through the fibroblast growth factor 13-mediated mitogen-activated protein kinase axis. | 0 |
| 37536293 | 2023 | A Heterozygous Variant of FGF13 Caused X-Linked Developmental and Epileptic Encephalopathy 90 in a Chinese Family. | 0 |
| 37603967 | 2023 | FGF13A interacts with NPM1 and UBF and inhibits the invasion of bladder cancer cells. | 0 |
| 36988403 | 2023 | The inhibitory role of microRNA-141-3p in human cutaneous melanoma growth and metastasis through the fibroblast growth factor 13-mediated mitogen-activated protein kinase axis. | 0 |
| 37536293 | 2023 | A Heterozygous Variant of FGF13 Caused X-Linked Developmental and Epileptic Encephalopathy 90 in a Chinese Family. | 0 |
| 37603967 | 2023 | FGF13A interacts with NPM1 and UBF and inhibits the invasion of bladder cancer cells. | 0 |
| 34871784 | 2022 | Further evidence of affected females with a heterozygous variant in FGF13 causing X-linked developmental and epileptic encephalopathy 90. | 4 |
| 36053411 | 2022 | FGF13 suppresses acute myeloid leukemia by regulating bone marrow niches. | 1 |
| 34871784 | 2022 | Further evidence of affected females with a heterozygous variant in FGF13 causing X-linked developmental and epileptic encephalopathy 90. | 4 |
| 36053411 | 2022 | FGF13 suppresses acute myeloid leukemia by regulating bone marrow niches. | 1 |
| 33245860 | 2021 | Missense variants in the N-terminal domain of the A isoform of FHF2/FGF13 cause an X-linked developmental and epileptic encephalopathy. | 10 |
| 33285262 | 2021 | Increased expression of fibroblast growth factor 13 in cortical lesions of the focal cortical dysplasia. | 0 |
| 33492380 | 2021 | FGF10 and FGF13 genetic variation and tooth-size discrepancies. | 1 |
Citation
Dessen P
FGF13 (fibroblast growth factor 13)
Atlas Genet Cytogenet Oncol Haematol. 2003-02-01
Online version: http://atlasgeneticsoncology.org/gene/40553/fgf13-(fibroblast-growth-factor-13)
