ILF3

Interleukin enhancer binding factor 3 Q12906 ILF3_HUMAN
Protein Coding Chr 19 19p13.2 Swiss-Prot reviewed Entrez 3609
Mutations
1,961
CL 286 · Tissue 1,622
Samples
423
CL 106 · Tissue 304
Peptides
364
unique mutant peptides
Transcripts
6
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
Mutations1,9612861,622
Samples423106304
Peptides36475277

Function

ILF3 · Interleukin enhancer binding factor 3

This gene encodes a double-stranded RNA (dsRNA) binding protein that complexes with other proteins, dsRNAs, small noncoding RNAs, and mRNAs to regulate gene expression and stabilize mRNAs. This protein (NF90, ILF3) forms a heterodimer with a 45 kDa transcription factor (NF45, ILF2) required for T-cell expression of interleukin 2. This complex has been shown to affect the redistribution of nuclear mRNA to the cytoplasm. Knockdown of NF45 or NF90 protein retards cell growth, possibly by inhibition of mRNA stabilization. In contrast, an isoform (NF110) of this gene that is predominantly restricted to the nucleus has only minor effects on cell growth when its levels are reduced. Alternative splicing results in multiple transcript variants encoding distinct isoforms.[provided by RefSeq, Dec 2014].

Isoforms & Proteins

6 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
ENST00000588657 Q12906-7 447 331
ENST00000590261 Q12906 374 298
ENST00000407004 Q12906-6 292 223
ENST00000589998 Q12906-2 290 222
ENST00000592763 Q12906-4 281 221
ENST00000250241 Q12906-5 277 218

Gene Properties

Type
Protein Coding
Chromosome
19
Cytoband
19p13.2
Entrez ID
Aliases
CBTFDRBFDRBP76MMP4MPHOSPH4MPP4

Recurrent Mutations

All 331 amino-acid changes on canonical ENST00000588657 · 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 ILF3 · 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 ILF3 – 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
11/40 28%
0/0 0%
Acute Monocytic Leukemia
0/1 0%
2/25 8%
Endometrial Carcinoma
12/42 29%
16/612 3%
Melanoma
9/210 4%
45/1899 2%
Thymic Epithelial Tumor
0/0 0%
1/39 3%
Acute Myeloid Leukemia
2/90 2%
0/0 0%
Colorectal Carcinoma
19/143 13%
53/3239 2%
Osteosarcoma
4/45 9%
0/166 0%
Oral Cavity Carcinoma
1/54 2%
0/0 0%
Hodgkins Lymphoma
0/16 0%
2/122 2%
Squamous Cell Lung Carcinoma
4/57 7%
8/810 1%
Bladder Carcinoma
1/58 2%
13/956 1%
Non-Small Cell Lung Carcinoma
9/304 3%
14/1390 1%
Gastric Carcinoma
4/74 5%
18/1809 1%
Germ Cell Tumour
0/25 0%
2/169 1%
Glioblastoma
1/98 1%
0/0 0%
Head and Neck Carcinoma
3/85 4%
14/1574 1%
Glioma
1/52 2%
19/2127 1%
Medulloblastoma
0/0 0%
4/450 1%
Small Cell Lung Carcinoma
0/9 0%
6/752 1%
Esophageal Carcinoma
2/23 9%
4/769 1%
Cervical Carcinoma
0/35 0%
3/422 1%
Other Sarcomas
2/69 3%
3/699 0%
Non-Cancerous
1/104 1%
5/830 1%
Other Solid Cancers
3/94 3%
7/1515 0%
Neuroendocrine Tumour
3/154 2%
1/577 0%
Prostate Carcinoma
2/13 15%
9/2105 0%
Biliary Tract Carcinoma
0/54 0%
5/950 1%
Breast Carcinoma
3/144 2%
14/3264 0%
Ovarian Carcinoma
1/109 1%
4/998 0%

Mutation Distribution

Where ILF3 is mutated · all tissues, split by cell line vs tissue

Mutation counts by tissue
Mutation Distribution

How many mutations in ILF3 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 1,961 mutations in ILF3

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