Basic information

Full name
fibroblast growth factor receptor 1
Ensembl
ENSG00000077782.21
Summary
The protein encoded by this gene is a member of the fibroblast growth factor receptor (FGFR) family, where amino acid sequence is highly conserved between members and throughout evolution. FGFR family members differ from one another in their ligand affinities and tissue distribution. A full-length representative protein consists of an extracellular region, composed of three immunoglobulin-like domains, a single hydrophobic membrane-spanning segment and a cytoplasmic tyrosine kinase domain. The extracellular portion of the protein interacts with fibroblast growth factors, setting in motion a cascade of downstream signals, ultimately influencing mitogenesis and differentiation. This particular family member binds both acidic and basic fibroblast growth factors and is involved in limb induction. Mutations in this gene have been associated with Pfeiffer syndrome, Jackson-Weiss syndrome, Antley-Bixler syndrome, osteoglophonic dysplasia, and autosomal dominant Kallmann syndrome 2. Chromosomal aberrations involving this gene are associated with stem cell myeloproliferative disorder and stem cell leukemia lymphoma syndrome. Alternatively spliced variants which encode different protein isoforms have been described; however, not all variants have been fully characterized. [provided by RefSeq, Jul 2008]
Annotation
Cancer driver (Oncogene) Druggable target (Tier T1) Protein Kinase Receptor

Protein product

  • ENST00000447712.7 Primary ENSP00000400162.2 (11 phosphosites)
  • ENST00000619564.3
  • ENST00000425967.7
  • ENST00000397091.9
  • ENST00000397113.6
  • ENST00000397108.8
  • ENST00000532791.5
  • ENST00000335922.9
  • ENST00000356207.9
  • ENST00000397103.5
  • ENST00000326324.10
  • ENST00000341462.8
Phosphosites on the primary protein product
Loading...

Tumor and normal comparison

Loading, please wait
Signed p-values
Data type
Meta P
BRCA
CCRCC
COAD
GBM
HNSCC
LSCC
LUAD
OV
PDAC
UCEC
RNA-8.5e-20-5.2e-3---1.6e-5-7.2e-8-7.2e-15--1.4e-8-
protein-2.7e-13-----0.001-3.9e-12-5.4e-5-1.3e-3-7.4e-43.2e-3

* P-values are from Wilcoxon rank sum test and can be clicked to show the box plots. Positive values mean higher abundance in tumor. BRCA and GBM do not have normal samples.

mRNA expression at gene level
BRCACCRCCCOADGBMHNSCCLSCCLUADOVPDACUCEC678910111213141516log2(RSEM+1)tumornormal
Protein expression
BRCACCRCCGBMHNSCCLSCCLUADOVPDACUCEC121314151617181920212223242526log2(MS1 intensity)tumornormal

* Mild outlier: filled circle; Extreme outlier: empty circle.

Phenotype and mutation association

Manhattan plot summarizing associations of phenotypes and mutations across all cohorts and omics data types

BRCACCRCCCOADGBMHNSCCLSCCLUADOVPDACUCEC02468101214161820222426280-2-4-6-8-10-12-14-16-18-20-22-24-26-28Pan-cancer0510152025303540450-5-10-15-20-25-30-35-40-45proteinRNASCNVclinicalpathwaycell typegenomicmutation-log10 of P-value

* Data points of significant associations above and below the dotted lines can be hovered to show the phenotype.

Associations of the protein abundance of FGFR1 with phenotypes and mutations

Loading, please wait
Signed p-values
Phenotype
Meta P
BRCA
CCRCC
COAD
GBM
HNSCC
LSCC
LUAD
OV
PDAC
UCEC
HALLMARK_HEDGEHOG_SIGNALING2.4e-102.9e-3--0.14-0.944.2e-33.8e-33.5e-32.9e-50.5
HALLMARK_MYOGENESIS5.3e-81.3e-8--0.32-0.141.3e-30.260.0112.1e-4-0.71
PROGENy: TGFb3e-74.5e-4---0.52-0.948.3e-40.027.7e-35.2e-5-0.49
xcell: Cancer associated fibroblast4.1e-72.5e-6--0.35-0.830.0230.160.0617.9e-5-0.54
HALLMARK_UV_RESPONSE_DN9.6e-74.4e-4--0.44-0.910.0130.0380.0665.3e-30.63
HALLMARK_EPITHELIAL_MESENCHYMAL_TRANSITION3.9e-61.1e-3---0.680.70.0030.360.0991.4e-5-0.96
HALLMARK_ANGIOGENESIS3.6e-56.6e-7---0.870.440.010.30.230.540.5
HALLMARK_TGF_BETA_SIGNALING4.0e-59.3e-4---0.85-0.350.0360.0335.4e-30.0170.97
xcell: stroma score1.5e-43.3e-5---0.17-0.310.0270.20.0923.6e-5-0.72
HALLMARK_APICAL_JUNCTION7.4e-42.7e-4---0.92-0.890.130.960.0472.7e-3-0.69
Showing 1 to 10 of 256 rows

* P-values could be from test for Spearman correlation, Wilcoxon rank sum test, Jonckheere-Terpstra trend test or Cox regression depending on the data type. P-values for individual cohorts can be clicked to show the data plots. The matrix icons in each row can be clicked to show a heatmap summary of associations across all cohorts and omics. The rows in the table can be expanded to show results from other omics.

Cis-association

Associations between omics data of FGFR1

BRCA0.660.190.35proteinmRNASCNVmethylationCCRCC-0.230.080.07proteinmRNASCNVmethylationCOAD0.05proteinmRNASCNVmethylationGBM0.55-0.21-0.07-0.290.19-0.13proteinmRNASCNVmethylationHNSCC0.22-0.16-0.03-0.360.100.03proteinmRNASCNVmethylationLSCC0.68-0.070.18-0.050.400.09proteinmRNASCNVmethylationLUAD0.490.030.19-0.410.17-0.00proteinmRNASCNVmethylationOV0.840.590.54proteinmRNASCNVmethylationPDAC0.51-0.04-0.04-0.150.110.13proteinmRNASCNVmethylationUCEC0.64-0.070.21-0.240.220.19proteinmRNASCNVmethylation

* The numbers are Spearman correlation coefficients and can be clicked to show the scatter plots. The color and size of the circles correlate with the coefficients.

Trans-association

Associations of the protein abundance of FGFR1 and the protein abundance of other genes

Loading, please wait
Signed p-values
Gene
Meta P
BRCA
CCRCC
COAD
GBM
HNSCC
LSCC
LUAD
OV
PDAC
UCEC
No matching records found

* P-values are from test for Spearman correlation. P-values for individual cohorts can be clicked to show the data plots. The matrix icons in each row can be clicked to show a heatmap summary of associations across all cohorts and omics. The rows in the table can be expanded to show results from other omics.

Gene set enrichment analysis

Submit genes and the common logarithm of the p-values of their association with to WebGestalt.