Basic information

Full name
angiogenin
Ensembl
ENSG00000214274.9
Summary
The protein encoded by this gene is a member of the RNase A superfamily though it has relatively weak ribonucleolytic activity. This protein is a potent mediator of new blood vessel formation and thus, in addition to the name RNase5, is commonly called angiogenin. This protein induces angiogenesis after binding to actin on the surface of endothelial cells. This protein also accumulates at the nucleolus where it stimulates ribosomal transcription. Under stress conditions this protein translocates to the cytosol where it hydrolyzes cellular tRNAs and influences protein synthesis. A signal peptide is cleaved from the precursor protein to produce a mature protein which contains a nuclear localization signal, a cell binding motif, and a catalytic domain. This protein has been shown to be both neurotrophic and neuroprotective and the mature protein has antimicrobial activity against some bacteria and fungi, including S. pneumoniae and C. albicans. Due to its effect on rRNA production and angiogenesis this gene plays important roles in cell growth and tumor progression. Mutations in this gene are associated with progression of amyotrophic lateral sclerosis (ALS). This gene and the neighboring RNase4 gene share promoters and 5' exons though each gene then splices to a distinct 3' exon containing the complete coding region of each gene. Alternative splicing results in multiple transcript variants encoding the same protein. [provided by RefSeq, Jul 2020]
Annotation
Ligand

Protein product

  • ENST00000336811.10 Primary ENSP00000336762.6 (0 phosphosite)
  • ENST00000397990.4
Phosphosites on the primary protein product
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Tumor and normal comparison

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Signed p-values
Data type
Meta P
BRCA
CCRCC
COAD
GBM
HNSCC
LSCC
LUAD
OV
PDAC
UCEC
RNA-9.1e-17-2e-10---4.9e-14-1.2e-31-2.4e-12-0.2-
protein-6.7e-42--1.8e-16-3.2e-17--5.7e-12-7.5e-18-1.3e-17-2.8e-41.4e-13-0.16

* 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
BRCACCRCCCOADGBMHNSCCLSCCLUADOVPDACUCEC456789101112log2(RSEM+1)tumornormal
Protein expression
BRCACCRCCCOADGBMHNSCCLSCCLUADOVPDACUCEC2122232425262728293031log2(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-cancer05101520253035404550550-5-10-15-20-25-30-35-40-45-50-55proteinRNASCNVclinicalpathwaycell 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 ANG with phenotypes and mutations

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Signed p-values
Phenotype
Meta P
BRCA
CCRCC
COAD
GBM
HNSCC
LSCC
LUAD
OV
PDAC
UCEC
HALLMARK_MYOGENESIS2.2e-562.2e-164.2e-32.2e-51.9e-36.4e-42.3e-81.7e-53e-76.3e-72.2e-16
PROGENy: TGFb1.2e-542.2e-162.1e-41.2e-73.1e-51.7e-61.0e-52.7e-41.3e-72.5e-64.6e-7
HALLMARK_EPITHELIAL_MESENCHYMAL_TRANSITION6.4e-485.5e-110.0147.7e-97.6e-91.3e-81.3e-47.9e-31.0e-65.4e-48.4e-7
xcell: stroma score8.8e-442.2e-161.5e-38.5e-44.3e-34.5e-31.3e-33.9e-67.1e-62.1e-92.8e-7
HALLMARK_UV_RESPONSE_DN1.5e-432.2e-160.0416.7e-65.3e-33.6e-57.9e-59.3e-66.0e-51.5e-58.4e-8
ESTIMATE: StromalScore7.2e-381.3e-100.0238.1e-64.7e-55.7e-59.6e-41.9e-32.5e-52.2e-43.4e-7
HALLMARK_APICAL_JUNCTION6.8e-329.1e-71.6e-33.0e-42.5e-43.7e-51.6e-40.175.3e-71.6e-41.8e-4
HALLMARK_TGF_BETA_SIGNALING2.3e-319.2e-92.2e-31.2e-64.3e-40.0277.4e-42.6e-52.3e-66.1e-30.016
xcell: Cancer associated fibroblast5.6e-312.4e-70.0171.2e-30.532.5e-31.9e-31.6e-51.2e-51.8e-72.3e-7
HALLMARK_ANGIOGENESIS2.7e-282.2e-160.0521.4e-79.4e-82.2e-40.0140.161.2e-4-0.413.7e-4
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 ANG

BRCA0.170.220.29proteinmRNASCNVmethylationCCRCC0.01-0.03-0.03-0.070.53-0.21proteinmRNASCNVmethylationCOAD-0.040.120.33proteinmRNASCNVmethylationGBM0.38-0.020.06-0.230.11-0.04proteinmRNASCNVmethylationHNSCC0.270.110.08-0.050.06-0.08proteinmRNASCNVmethylationLSCC0.40-0.230.04-0.010.320.07proteinmRNASCNVmethylationLUAD0.260.04-0.030.170.060.10proteinmRNASCNVmethylationOV0.160.190.26proteinmRNASCNVmethylationPDAC0.170.040.23-0.030.17-0.14proteinmRNASCNVmethylationUCEC0.17-0.000.01-0.21-0.070.02proteinmRNASCNVmethylation

* 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 ANG and the protein abundance of other genes

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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.