FGF13
fibroblast growth factor 13 | FGF2, FHF2, FLJ30672, LINC00889

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 gene is located in a region on chromosome X, which is associated with Borjeson-Forssman-Lehmann syndrome (BFLS), making it a possible candidate gene for familial cases of the BFLS, and for other syndromal and nonspecific forms of X-linked cognitive disability mapping to this region. Alternative splicing of this gene at the 5' end results in several transcript variants encoding different isoforms with different N-termini. [provided by RefSeq, Nov 2008]

Member of: DE-3 DE-3.36 Developmental clusters: GC6
Biological processes 72 terms
MAPK cascade (GO:0000165)axon (GO:0030424)axon (GO:0030424)beta-tubulin binding (GO:0048487)beta-tubulin binding (GO:0048487)cell-cell signaling (GO:0007267)cell-cell signaling (GO:0007267)cerebral cortex cell migration (GO:0021795)cerebral cortex cell migration (GO:0021795)cytoplasm (GO:0005737)cytoplasm (GO:0005737)cytoplasm (GO:0005737)cytosol (GO:0005829)cytosol (GO:0005829)dendrite (GO:0030425)dendrite (GO:0030425)establishment of neuroblast polarity (GO:0045200)filopodium (GO:0030175)filopodium (GO:0030175)growth cone (GO:0030426)growth cone (GO:0030426)growth factor activity (GO:0008083)growth factor activity (GO:0008083)hippocampus development (GO:0021766)hippocampus development (GO:0021766)inhibitory synapse assembly (GO:1904862)inhibitory synapse assembly (GO:1904862)intercalated disc (GO:0014704)intercalated disc (GO:0014704)lateral plasma membrane (GO:0016328)lateral plasma membrane (GO:0016328)learning (GO:0007612)learning (GO:0007612)memory (GO:0007613)memory (GO:0007613)microtubule (GO:0005874)microtubule (GO:0005874)microtubule binding (GO:0008017)microtubule binding (GO:0008017)microtubule polymerization (GO:0046785)microtubule polymerization (GO:0046785)negative regulation of collateral sprouting (GO:0048671)negative regulation of microtubule depolymerization (GO:0007026)negative regulation of microtubule depolymerization (GO:0007026)nervous system development (GO:0007399)nervous system development (GO:0007399)neurogenesis (GO:0022008)neuron migration (GO:0001764)neuron projection (GO:0043005)neuron projection (GO:0043005)nucleus (GO:0005634)nucleus (GO:0005634)nucleus (GO:0005634)nucleus (GO:0005634)plasma membrane (GO:0005886)plasma membrane (GO:0005886)positive regulation of voltage-gated sodium channel activity (GO:1905152)protein binding (GO:0005515)protein localization to plasma membrane (GO:0072659)protein localization to plasma membrane (GO:0072659)regulation of cardiac muscle cell action potential involved in regulation of contraction (GO:0098909)regulation of cardiac muscle cell action potential involved in regulation of contraction (GO:0098909)sarcolemma (GO:0042383)signal transduction (GO:0007165)sodium channel regulator activity (GO:0017080)sodium channel regulator activity (GO:0017080)sodium channel regulator activity (GO:0017080)sodium channel regulator activity (GO:0017080)sodium ion transport (GO:0006814)sodium ion transport (GO:0006814)transmembrane transporter binding (GO:0044325)transmembrane transporter binding (GO:0044325)
Expression (TPM)
FGF13 — as a Regulated Gene

TFs regulating FGF13 0 TFs

Transcription factors with Perturb-seq knockdown data for FGF13. The Binding column indicates whether any binding evidence exists for this TF–gene pair (ChIP-seq or motif footprint peaks). The Mean coef is the average Perturb-seq regression coefficient across active gRNAs (positive = FGF13 upregulated upon KD; negative = downregulated). The Outlier column indicates whether this gene is in the top or bottom 5% of all TF knockdown effects.

Data: Effect:
TF Mean coef Binding Outlier TF→Gene link

Elements linked to FGF13

Open chromatin peaks (ATAC-seq) in the genomic neighbourhood of FGF13, linked by TSS proximity or chromatin conformation (Multiome / HiCAR). Each element overlaps at least one TF ChIP-seq binding site — the TFs column shows how many distinct TFs bind that element.

Accessibility Element Dist. to TSS Link type TFs
chrX:138,269,675–138,270,410 441.7 kb Distal (>10kb) Multiome HiCAR 34
chrX:138,710,307–138,710,745 971 bp At TSS 60
chrX:138,710,875–138,711,289 427 bp At TSS 84
chrX:138,711,385–138,712,390 161 bp At TSS Multiome 253
chrX:139,194,606–139,195,039 10.0 kb Proximal (<10kb) 225
chrX:139,202,708–139,204,646 376 bp At TSS 239
chrX:139,204,746–139,205,746 493.5 kb Distal (>10kb) Multiome 326
chrX:139,206,148–139,206,592 1.1 kb Proximal (<10kb) 50
chrX:139,211,514–139,211,955 6.5 kb Proximal (<10kb) 81

Genome Browser

Genomic view of the FGF13 locus showing ATAC-seq accessibility and RNA-seq expression across the ESC → DE time course, together with TF binding peaks and element-to-TSS loop connections.

chrX:138,259,675 – 139,221,955
Proximal 1 kb Distal 10 kb Multiome HiCAR ATAC-seq RNA-seq