CTIF

Cap binding complex dependent translation initiation factor O43310 CTIF_HUMAN
Protein Coding Chr 18 18q21.1 Swiss-Prot reviewed Entrez 9811
Mutations
596
CL 76 · Tissue 516
Samples
301
CL 51 · Tissue 248
Peptides
231
unique mutant peptides
Transcripts
2
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
Mutations59676516
Samples30151248
Peptides23134201

Function

CTIF · Cap binding complex dependent translation initiation factor

CTIF is a component of the CBP80 (NCBP1; MIM 600469)/CBP20 (NCBP2; MIM 605133) translation initiation complex that binds cotranscriptionally to the cap end of nascent mRNA. The CBP80/CBP20 complex is involved in a simultaneous editing and translation step that recognizes premature termination codons (PTCs) in mRNAs and directs PTC-containing mRNAs toward nonsense-mediated decay (NMD). On mRNAs without PTCs, the CBP80/CBP20 complex is replaced with cytoplasmic mRNA cap-binding proteins, including EIF4G (MIM 600495), and steady-state translation of the mRNAs resumes in the cytoplasm (Kim et al., 2009 [PubMed 19648179]).[supplied by OMIM, Dec 2009].

Isoforms & Proteins

2 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
ENST00000256413 O43310 316 221
ENST00000382998 O43310-2 280 205

Gene Properties

Type
Protein Coding
Chromosome
18
Cytoband
18q21.1
Entrez ID
Aliases
Gm672KIAA0427

Recurrent Mutations

All 220 amino-acid changes on canonical ENST00000256413 · 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 CTIF · 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 CTIF – 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%
Chronic Myelogenous Leukemia
1/25 4%
0/0 0%
Endometrial Carcinoma
3/42 7%
20/612 3%
Acute Myeloid Leukemia
2/90 2%
0/0 0%
Melanoma
7/210 3%
37/1899 2%
Gastric Carcinoma
2/74 3%
24/1809 1%
Other Solid Cancers
0/94 0%
22/1515 1%
Colorectal Carcinoma
5/143 4%
35/3239 1%
Squamous Cell Lung Carcinoma
2/57 4%
8/810 1%
Germ Cell Tumour
0/25 0%
2/169 1%
Glioblastoma
1/98 1%
0/0 0%
Esophageal Carcinoma
0/23 0%
7/769 1%
Cervical Carcinoma
0/35 0%
4/422 1%
Hodgkins Lymphoma
0/16 0%
1/122 1%
Non-Small Cell Lung Carcinoma
6/304 2%
6/1390 0%
Head and Neck Carcinoma
0/85 0%
10/1574 1%
Neuroendocrine Tumour
2/154 1%
2/577 0%
Other Sarcomas
2/69 3%
2/699 0%
Biliary Tract Carcinoma
1/54 2%
4/950 0%
Esophageal Squamous Cell Carcinoma
1/51 2%
11/2550 0%
Ovarian Carcinoma
1/109 1%
4/998 0%
Bladder Carcinoma
0/58 0%
4/956 0%
Glioma
0/52 0%
8/2127 0%
Breast Carcinoma
4/144 3%
8/3264 0%
Hepatocellular Carcinoma
0/46 0%
8/2210 0%
B-Cell Non-Hodgkins Lymphoma
3/88 3%
5/2534 0%
Plasma Cell Myeloma
1/44 2%
0/305 0%
Small Cell Lung Carcinoma
0/9 0%
2/752 0%
Kidney Carcinoma
0/85 0%
5/1862 0%
Prostate Carcinoma
2/13 15%
2/2105 0%

Mutation Distribution

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

Mutation counts by tissue
Mutation Distribution

How many mutations in CTIF 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 596 mutations in CTIF

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