CIRBP

Cold inducible RNA binding protein Q14011 CIRBP_HUMAN
Protein Coding Chr 19 19p13.3 Swiss-Prot reviewed Entrez 1153
Mutations
1,678
CL 227 · Tissue 1,381
Samples
162
CL 41 · Tissue 115
Peptides
145
unique mutant peptides
Transcripts
14
isoforms mutated

Stats by Source

Total, split by cell line (COSMIC CL / DepMap / PubMed) vs tissue (COSMIC primary tissue)

How the counts split by source
Stats by Source

Total = all mutations for this gene across every source.

Cell line = COSMIC Cell Lines Project + DepMap + PubMed.

Tissue = COSMIC primary-tissue (patient tumour) samples.

Total can exceed cell line + tissue: COSMIC tissue-derived models sit only in global, and a peptide can be shared across both.

TotalCell lineTissue
Mutations1,6782271,381
Samples16241115
Peptides14533112

Function

CIRBP · Cold inducible RNA binding protein

Enables mRNA 3'-UTR binding activity and small ribosomal subunit rRNA binding activity. Involved in mRNA stabilization; positive regulation of translation; and response to UV. Located in cytoplasm and nucleoplasm. [provided by Alliance of Genome Resources, Apr 2022]

Isoforms & Proteins

14 transcripts · UniProt mapping is sequence-verified (AA-safe)

About the isoform mapping
Isoforms & Proteins

Each Ensembl transcript (ENST) this gene is mutated on, with its matched UniProt accession.

The mapping is sequence-verified: the UniProt sequence is identical to the transcript translation, so amino-acid positions line up exactly. A * marks an unreviewed (TrEMBL) entry.

Counts are mutations and unique mutant peptides on each transcript.

TranscriptUniProtMutationsPeptides
ENST00000587896 D6W5Y5* 172 119
ENST00000587323 D6W5Y5* 143 107
ENST00000588230 D6W5Y5* 143 107
ENST00000589710 D6W5Y5* 143 107
ENST00000628979 D6W5Y5* 143 107
ENST00000413636 Q14011-2 113 89
ENST00000320936 Q14011 103 72
ENST00000585630 Q14011 103 72
ENST00000586472 Q14011 103 72
ENST00000588030 Q14011 103 72
ENST00000588090 Q14011 103 72
ENST00000586773 K7EPM4* 102 71
ENST00000589235 K7EPM4* 102 71
ENST00000591935 K7EPM4* 102 71

Gene Properties

Type
Protein Coding
Chromosome
19
Cytoband
19p13.3
Entrez ID
Aliases
CIRP

Recurrent Mutations

All 89 amino-acid changes on canonical ENST00000413636 · needle height = samples · drag the mini-map to zoom

What this lollipop shows
Recurrent Mutations

A lollipop / needle plot – the standard way to show recurrent mutations along a protein (as used by cBioPortal and MutationMapper).

X-axis = amino-acid position in the protein.

Needle height & head size = how often that exact amino-acid change was observed (its recurrence). Tall/large heads are mutational hotspots.

The most recurrent changes are labelled; hover any needle for the change, position and counts.

Mutation frequency across cancer types

% of samples with a missense/complex mutation in CIRBP · cell line vs tissue

How this frequency is counted
Cancer-type mutation frequency

For each cancer type, the fraction of samples that carry at least one missense/complex mutation anywhere in CIRBP – counted as distinct samples (a sample counts once no matter how many mutations it has).

Split into cell line and tissue; each cell shows mutated / total and the percentage. Cohorts with <20 samples are omitted. Ordered by combined frequency.

Cancer typeCell linesTissue samples
T-Lymphoblastic Leukemia
4/40 10%
0/0 0%
Chondrosarcoma
2/14 14%
0/75 0%
Endometrial Carcinoma
5/42 12%
8/612 1%
Glioblastoma
1/98 1%
0/0 0%
Colorectal Carcinoma
10/143 7%
20/3239 1%
Gastric Carcinoma
0/74 0%
11/1809 1%
Hepatocellular Carcinoma
0/46 0%
12/2210 1%
Cervical Carcinoma
0/35 0%
2/422 0%
Melanoma
3/210 1%
6/1899 0%
Non-Small Cell Lung Carcinoma
3/304 1%
4/1390 0%
Glioma
2/52 4%
7/2127 0%
Breast Carcinoma
2/144 1%
11/3264 0%
Esophageal Squamous Cell Carcinoma
0/51 0%
9/2550 0%
Squamous Cell Lung Carcinoma
0/57 0%
3/810 0%
Ewings Sarcoma
0/63 0%
1/262 0%
Plasma Cell Myeloma
0/44 0%
1/305 0%
Neuroendocrine Tumour
0/154 0%
2/577 0%
Ovarian Carcinoma
3/109 3%
0/998 0%
Other Solid Cancers
0/94 0%
4/1515 0%
Head and Neck Carcinoma
0/85 0%
4/1574 0%
Medulloblastoma
0/0 0%
1/450 0%
Biliary Tract Carcinoma
1/54 2%
1/950 0%
Kidney Carcinoma
0/85 0%
3/1862 0%
B-Cell Non-Hodgkins Lymphoma
0/88 0%
4/2534 0%
Esophageal Carcinoma
0/23 0%
1/769 0%
Small Cell Lung Carcinoma
0/9 0%
1/752 0%
B-Lymphoblastic Leukemia
3/55 5%
0/2640 0%
Non-Cancerous
0/104 0%
1/830 0%
Bladder Carcinoma
0/58 0%
1/956 0%
Prostate Carcinoma
0/13 0%
2/2105 0%

Mutation Distribution

Where CIRBP is mutated · all tissues, split by cell line vs tissue

Mutation counts by tissue
Mutation Distribution

How many mutations in CIRBP were found in each tissue, across the whole database.

Each bar is a tissue (cell-line and tissue names are merged to the standard tissue), split into cell line and tissue (patient tumour) contributions.

This shows the cancer-context where this gene is recurrently altered.

GTEx Expression

Median TPM across 54 healthy tissues

GTEx Portal ↗
About the expression data
GTEx Expression

Median gene expression (TPM) in normal, non-cancer human tissues from the GTEx project.

Useful for judging tumour specificity – a strong neoantigen target ideally comes from a gene with low expression in healthy tissues.

Scroll or drag the mini-axis below the chart to browse all tissues.

Mutations

All 1,678 mutations in CIRBP

About the mutation list
Mutations

Every mutation record for this gene, across all samples and sources.

The Sample column links to the cell line (cell-line samples) or the tissue type (tissue samples).

Use the Type / Source filters, the search box, and column sorting to explore; each CAN-IMMUNE ID opens the full mutation & peptide view.

IDSampleTranscriptAA Change CDSTypeSourceMutant PeptideWild-type Peptide