KANK4

KN motif and ankyrin repeat domains 4 Q5T7N3 KANK4_HUMAN
Protein Coding Chr 1 1p31.3 Swiss-Prot reviewed Entrez 163782
Mutations
1,411
CL 245 · Tissue 1,149
Samples
705
CL 172 · Tissue 525
Peptides
529
unique mutant peptides
Transcripts
4
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
Mutations1,4112451,149
Samples705172525
Peptides529118433

Function

KANK4 · KN motif and ankyrin repeat domains 4

Predicted to be involved in negative regulation of actin filament polymerization. Located in cytosol and microtubule cytoskeleton. [provided by Alliance of Genome Resources, Apr 2022]

Isoforms & Proteins

4 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
ENST00000371153 Q5T7N3 793 509
ENST00000354381 Q5T7N3-2 273 170
ENST00000371150 B1ALP6* 257 159
ENST00000317477 B1ALP5* 88 59

Gene Properties

Type
Protein Coding
Chromosome
1
Cytoband
1p31.3
Entrez ID
Aliases
ANKRD38dJ1078M7.1

Recurrent Mutations

All 509 amino-acid changes on canonical ENST00000371153 · 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 KANK4 · 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 KANK4 – 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%
Glioblastoma
8/98 8%
0/0 0%
Melanoma
17/210 8%
143/1899 8%
Gastrointestinal Stromal Tumour
0/0 0%
6/133 5%
T-Cell Non-Hodgkins Lymphoma
1/26 4%
0/0 0%
Endometrial Carcinoma
4/42 10%
21/612 3%
Non-Small Cell Lung Carcinoma
20/304 7%
42/1390 3%
Thymic Epithelial Tumor
0/0 0%
1/39 3%
Other Solid Cancers
6/94 6%
35/1515 2%
Squamous Cell Lung Carcinoma
6/57 11%
16/810 2%
Hodgkins Lymphoma
2/16 12%
1/122 1%
Bladder Carcinoma
1/58 2%
21/956 2%
Gastric Carcinoma
6/74 8%
34/1809 2%
Neuroendocrine Tumour
13/154 8%
2/577 0%
Colorectal Carcinoma
22/143 15%
42/3239 1%
Germ Cell Tumour
2/25 8%
1/169 1%
Plasma Cell Myeloma
4/44 9%
1/305 0%
Burkitts Lymphoma
3/32 9%
0/196 0%
Small Cell Lung Carcinoma
0/9 0%
10/752 1%
Other Sarcomas
5/69 7%
5/699 1%
Biliary Tract Carcinoma
1/54 2%
12/950 1%
Chondrosarcoma
1/14 7%
0/75 0%
Acute Myeloid Leukemia
1/90 1%
0/0 0%
Non-Cancerous
0/104 0%
9/830 1%
Mesothelioma
2/62 3%
0/165 0%
Cervical Carcinoma
0/35 0%
4/422 1%
Adrenocortical Carcinoma
0/3 0%
1/112 1%
Glioma
3/52 6%
15/2127 1%
Thyroid Gland Carcinoma
1/45 2%
12/1592 1%
Head and Neck Carcinoma
2/85 2%
11/1574 1%

Mutation Distribution

Where KANK4 is mutated · all tissues, split by cell line vs tissue

Mutation counts by tissue
Mutation Distribution

How many mutations in KANK4 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 53 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 1,411 mutations in KANK4

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