TRAK1

Trafficking kinesin protein 1 Q9UPV9 TRAK1_HUMAN
Protein Coding Chr 3 3p22.1 Swiss-Prot reviewed Entrez 22906
Mutations
2,446
CL 332 · Tissue 2,032
Samples
529
CL 111 · Tissue 411
Peptides
425
unique mutant peptides
Transcripts
8
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
Mutations2,4463322,032
Samples529111411
Peptides42566347

Function

TRAK1 · Trafficking kinesin protein 1

Predicted to enable GABA receptor binding activity and myosin binding activity. Involved in endosome to lysosome transport. Located in early endosome and mitochondrion. Implicated in developmental and epileptic encephalopathy 68. [provided by Alliance of Genome Resources, Apr 2022]

Isoforms & Proteins

8 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
ENST00000327628 Q9UPV9 493 349
ENST00000396175 C9JC32* 424 319
ENST00000487159 A0A0D9SFL5* 404 305
ENST00000341421 Q9UPV9-2 321 232
ENST00000613405 A0A087X0N0* 308 223
ENST00000449246 Q9UPV9-3 251 180
ENST00000484786 A0A0D9SGH2* 244 175
ENST00000673621 A0A5F9ZI06* 1 1

Gene Properties

Type
Protein Coding
Chromosome
3
Cytoband
3p22.1
Entrez ID
Aliases
DEE68EIEE68MILT1OIP106

Recurrent Mutations

All 349 amino-acid changes on canonical ENST00000327628 · 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 TRAK1 · 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 TRAK1 – 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
10/42 24%
29/612 5%
Acute Myeloid Leukemia
4/90 4%
0/0 0%
Colorectal Carcinoma
21/143 15%
82/3239 3%
Melanoma
10/210 5%
49/1899 3%
Burkitts Lymphoma
3/32 9%
3/196 2%
T-Lymphoblastic Leukemia
1/40 2%
0/0 0%
Gastric Carcinoma
3/74 4%
35/1809 2%
Bladder Carcinoma
2/58 3%
17/956 2%
Oral Cavity Carcinoma
1/54 2%
0/0 0%
Mesothelioma
4/62 6%
0/165 0%
Other Solid Cancers
2/94 2%
26/1515 2%
Non-Small Cell Lung Carcinoma
17/304 6%
12/1390 1%
Osteosarcoma
2/45 4%
1/166 1%
Ovarian Carcinoma
7/109 6%
7/998 1%
Thyroid Gland Carcinoma
1/45 2%
18/1592 1%
Squamous Cell Lung Carcinoma
1/57 2%
9/810 1%
Neuroendocrine Tumour
3/154 2%
5/577 1%
Cervical Carcinoma
0/35 0%
5/422 1%
Germ Cell Tumour
1/25 4%
1/169 1%
Hepatocellular Carcinoma
3/46 7%
17/2210 1%
Esophageal Carcinoma
0/23 0%
7/769 1%
Non-Cancerous
1/104 1%
6/830 1%
Gastrointestinal Stromal Tumour
0/0 0%
1/133 1%
Head and Neck Carcinoma
2/85 2%
9/1574 1%
Esophageal Squamous Cell Carcinoma
2/51 4%
15/2550 1%
Ewings Sarcoma
0/63 0%
2/262 1%
Biliary Tract Carcinoma
1/54 2%
5/950 1%
Other Sarcomas
0/69 0%
4/699 1%
Glioma
3/52 6%
8/2127 0%
Breast Carcinoma
3/144 2%
13/3264 0%

Mutation Distribution

Where TRAK1 is mutated · all tissues, split by cell line vs tissue

Mutation counts by tissue
Mutation Distribution

How many mutations in TRAK1 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 2,446 mutations in TRAK1

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