KIF11

Kinesin family member 11 P52732 KIF11_HUMAN
Protein Coding Chr 10 10q23.33 Swiss-Prot reviewed Entrez 3832
Mutations
318
CL 56 · Tissue 257
Samples
293
CL 52 · Tissue 238
Peptides
266
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
Mutations31856257
Samples29352238
Peptides26639225

Function

KIF11 · Kinesin family member 11

This gene encodes a motor protein that belongs to the kinesin-like protein family. Members of this protein family are known to be involved in various kinds of spindle dynamics. The function of this gene product includes chromosome positioning, centrosome separation and establishing a bipolar spindle during cell mitosis. [provided by RefSeq, Jul 2008].

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
ENST00000260731 P52732 317 265
ENST00000676757 A0A7I2V3A9* 1 1

Gene Properties

Type
Protein Coding
Chromosome
10
Cytoband
10q23.33
Entrez ID
Aliases
EG5HKSPKNSL1MCLMRTRIP5

Recurrent Mutations

All 265 amino-acid changes on canonical ENST00000260731 · 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 KIF11 · 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 KIF11 – 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
Endometrial Carcinoma
8/42 19%
26/612 4%
Oral Cavity Carcinoma
2/54 4%
0/0 0%
T-Lymphoblastic Leukemia
1/40 2%
0/0 0%
Hodgkins Lymphoma
3/16 19%
0/122 0%
Non-Small Cell Lung Carcinoma
9/304 3%
14/1390 1%
Burkitts Lymphoma
2/32 6%
1/196 1%
Cervical Carcinoma
0/35 0%
6/422 1%
Melanoma
3/210 1%
23/1899 1%
Colorectal Carcinoma
3/143 2%
36/3239 1%
Acute Myeloid Leukemia
1/90 1%
0/0 0%
Bladder Carcinoma
0/58 0%
10/956 1%
Non-Cancerous
0/104 0%
7/830 1%
Squamous Cell Lung Carcinoma
2/57 4%
4/810 0%
Other Solid Cancers
1/94 1%
10/1515 1%
Gastric Carcinoma
0/74 0%
12/1809 1%
Biliary Tract Carcinoma
1/54 2%
5/950 1%
Plasma Cell Myeloma
1/44 2%
1/305 0%
Other Sarcomas
1/69 1%
3/699 0%
Thyroid Gland Carcinoma
2/45 4%
6/1592 0%
Head and Neck Carcinoma
1/85 1%
7/1574 0%
Osteosarcoma
1/45 2%
0/166 0%
Breast Carcinoma
0/144 0%
16/3264 0%
Kidney Carcinoma
0/85 0%
9/1862 0%
Mesothelioma
1/62 2%
0/165 0%
Neuroendocrine Tumour
2/154 1%
1/577 0%
Hepatocellular Carcinoma
0/46 0%
9/2210 0%
Glioma
0/52 0%
8/2127 0%
Ovarian Carcinoma
1/109 1%
3/998 0%
Ewings Sarcoma
1/63 2%
0/262 0%
Esophageal Squamous Cell Carcinoma
1/51 2%
7/2550 0%

Mutation Distribution

Where KIF11 is mutated · all tissues, split by cell line vs tissue

Mutation counts by tissue
Mutation Distribution

How many mutations in KIF11 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 318 mutations in KIF11

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