IKZF2

IKAROS family zinc finger 2 Q9UKS7 IKZF2_HUMAN
Protein Coding Chr 2 2q34 Swiss-Prot reviewed Entrez 22807
Mutations
1,725
CL 231 · Tissue 1,481
Samples
375
CL 65 · Tissue 306
Peptides
340
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
Mutations1,7252311,481
Samples37565306
Peptides34049295

Function

IKZF2 · IKAROS family zinc finger 2

This gene encodes a member of the Ikaros family of zinc-finger proteins. Three members of this protein family (Ikaros, Aiolos and Helios) are hematopoietic-specific transcription factors involved in the regulation of lymphocyte development. This protein forms homo- or hetero-dimers with other Ikaros family members, and is thought to function predominantly in early hematopoietic development. Multiple transcript variants encoding different isoforms have been found for this gene, but the biological validity of some variants has not been determined. [provided by RefSeq, Jul 2008].

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
ENST00000434687 Q9UKS7 396 279
ENST00000342002 B4DWF2* 359 268
ENST00000374319 Q9UKS7-2 346 256
ENST00000457361 A0A0A0MT14* 310 230
ENST00000451136 A0A0A0MSL2* 292 212
ENST00000442445 E7ES26* 22 18

Gene Properties

Type
Protein Coding
Chromosome
2
Cytoband
2q34
Entrez ID
Aliases
ANF1A2HELIOSICHADIMDIAZNF1A2ZNFN1A2

Recurrent Mutations

All 279 amino-acid changes on canonical ENST00000434687 · 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 IKZF2 · 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 IKZF2 – 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
Melanoma
6/210 3%
85/1899 4%
Chronic Myelogenous Leukemia
1/25 4%
0/0 0%
Acute Myeloid Leukemia
3/90 3%
0/0 0%
Endometrial Carcinoma
5/42 12%
12/612 2%
T-Lymphoblastic Leukemia
1/40 2%
0/0 0%
Bladder Carcinoma
2/58 3%
21/956 2%
Glioblastoma
2/98 2%
0/0 0%
Hodgkins Lymphoma
2/16 12%
0/122 0%
Colorectal Carcinoma
3/143 2%
36/3239 1%
Neuroendocrine Tumour
4/154 3%
4/577 1%
Germ Cell Tumour
1/25 4%
1/169 1%
Non-Small Cell Lung Carcinoma
2/304 1%
14/1390 1%
Squamous Cell Lung Carcinoma
3/57 5%
5/810 1%
Ewings Sarcoma
0/63 0%
3/262 1%
Burkitts Lymphoma
2/32 6%
0/196 0%
Other Solid Cancers
0/94 0%
14/1515 1%
Gastric Carcinoma
0/74 0%
16/1809 1%
Other Sarcomas
1/69 1%
5/699 1%
Non-Cancerous
1/104 1%
6/830 1%
Esophageal Squamous Cell Carcinoma
2/51 4%
16/2550 1%
Cervical Carcinoma
0/35 0%
3/422 1%
Ovarian Carcinoma
3/109 3%
3/998 0%
Hepatocellular Carcinoma
2/46 4%
10/2210 0%
Biliary Tract Carcinoma
1/54 2%
4/950 0%
Breast Carcinoma
4/144 3%
11/3264 0%
Mesothelioma
1/62 2%
0/165 0%
Thyroid Gland Carcinoma
2/45 4%
5/1592 0%
Kidney Carcinoma
1/85 1%
7/1862 0%
Head and Neck Carcinoma
1/85 1%
5/1574 0%
B-Cell Non-Hodgkins Lymphoma
5/88 6%
4/2534 0%

Mutation Distribution

Where IKZF2 is mutated · all tissues, split by cell line vs tissue

Mutation counts by tissue
Mutation Distribution

How many mutations in IKZF2 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 1,725 mutations in IKZF2

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