Basic information

Full name
factor interacting with PAPOLA and CPSF1
Ensembl
ENSG00000145216.16
Summary
This gene encodes a subunit of the CPSF (cleavage and polyadenylation specificity factor) complex that polyadenylates the 3' end of mRNA precursors. This gene, the homolog of yeast Fip1 (factor interacting with PAP), binds to U-rich sequences of pre-mRNA and stimulates poly(A) polymerase activity. Its N-terminus contains a PAP-binding site and its C-terminus an RNA-binding domain. An interstitial chromosomal deletion on 4q12 creates an in-frame fusion of human genes FIP1L1 and PDGFRA (platelet-derived growth factor receptor, alpha). The FIP1L1-PDGFRA fusion gene encodes a constitutively activated tyrosine kinase that joins the first 233 amino acids of FIP1L1 to the last 523 amino acids of PDGFRA. This gene fusion and chromosomal deletion is the cause of some forms of idiopathic hypereosinophilic syndrome (HES). This syndrome, recently reclassified as chronic eosinophilic leukemia (CEL), is responsive to treatment with tyrosine kinase inhibitors. Alternative splicing results in multiple transcript variants encoding distinct isoforms. [provided by RefSeq, Oct 2008]
Annotation
Essential genes

Protein product

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
RNA1.7e-13-1.3e-12--3.5e-36.4e-7-0.33-0.014-
protein2.5e-70-0.0421.4e-22-4.4e-176.3e-302.1e-293.7e-10-0.380.055

* 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
BRCACCRCCCOADGBMHNSCCLSCCLUADOVPDACUCEC99.51010.51111.51212.51313.51414.5log2(RSEM+1)tumornormal
Protein expression
BRCACCRCCCOADGBMHNSCCLSCCLUADOVPDACUCEC2222.52323.52424.52525.52626.5log2(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

BRCACCRCCCOADGBMHNSCCLSCCLUADOVPDACUCEC02468101214160-2-4-6-8-10-12-14-16Pan-cancer0246810121416182022242628300-2-4-6-8-10-12-14-16-18-20-22-24-26-28-30proteinRNASCNVclinicalpathwaycell 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 FIP1L1 with phenotypes and mutations

Loading, please wait
Signed p-values
Phenotype
Meta P
BRCA
CCRCC
COAD
GBM
HNSCC
LSCC
LUAD
OV
PDAC
UCEC
HALLMARK_SPERMATOGENESIS1.3e-210.0110.350.177.8e-42.2e-163.4e-70.0836.8e-30.210.003
Tumor Purity (ABSOLUTE)1.4e-191.3e-30.911.5e-41.4e-55.6e-53.9e-60.570.0360.0119.6e-4
HALLMARK_E2F_TARGETS1.5e-180.0360.50.212e-82.0e-68.3e-70.460.140.0541.3e-5
chromosomal instability1.2e-161.7e-30.972.1e-41.0e-41.8e-54.5e-70.180.10.180.072
HALLMARK_G2M_CHECKPOINT4e-160.0990.0980.611.7e-72.7e-41.7e-50.340.190.064.4e-6
KINASE-PSP_CDK24.2e-160.360.583.5e-39.0e-61.3e-60.0140.70.0590.0159.9e-7
HALLMARK_MYC_TARGETS_V29.1e-146.6e-3-0.50.254.6e-47.8e-35.8e-50.0461.7e-30.211.4e-4
Tumor Purity (WGS)3.9e-10-0.45-2.6e-82.5e-57.1e-50.054--0.360.31
HALLMARK_MYC_TARGETS_V16.3e-100.056-0.290.0880.0010.172.0e-50.140.0440.0270.018
xcell: T cell CD4+ Th13e-93.4e-3-0.90.161e-70.159.1e-50.038-0.9-0.191.1e-3
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 FIP1L1

BRCA0.350.210.40proteinmRNASCNVmethylationCCRCC0.03-0.070.01-0.130.470.16proteinmRNASCNVmethylationCOAD0.23-0.000.37proteinmRNASCNVmethylationGBM0.590.020.280.050.41-0.16proteinmRNASCNVmethylationHNSCC0.320.040.17-0.160.63-0.25proteinmRNASCNVmethylationLSCC0.65-0.080.36-0.120.62-0.06proteinmRNASCNVmethylationLUAD0.48-0.100.33-0.120.59-0.15proteinmRNASCNVmethylationOV0.450.400.69proteinmRNASCNVmethylationPDAC0.030.060.01-0.110.57-0.26proteinmRNASCNVmethylationUCEC0.13-0.14-0.070.010.28-0.05proteinmRNASCNVmethylation

* 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 FIP1L1 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.