TDRD15

Tudor domain containing 15 B5MCY1 TDR15_HUMAN
Protein Coding Chr 2 2p24.1 Swiss-Prot reviewed Entrez 100129278
Mutations
1,220
CL 495 · Tissue 708
Samples
580
CL 265 · Tissue 306
Peptides
472
unique mutant peptides
Transcripts
3
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
Mutations1,220495708
Samples580265306
Peptides472191288

Isoforms & Proteins

3 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
ENST00000405799 B5MCY1 690 471
ENST00000622654 B5MCY1 529 423
ENST00000707967 B5MCY1 1 1

Gene Properties

Type
Protein Coding
Chromosome
2
Cytoband
2p24.1
Entrez ID

Recurrent Mutations

All 471 amino-acid changes on canonical ENST00000405799 · 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 TDRD15 · 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 TDRD15 – 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
Chronic Myelogenous Leukemia
5/25 20%
0/0 0%
T-Lymphoblastic Leukemia
7/40 18%
0/0 0%
Oral Cavity Carcinoma
9/54 17%
0/0 0%
T-Cell Non-Hodgkins Lymphoma
3/26 12%
0/0 0%
Acute Myeloid Leukemia
6/90 7%
0/0 0%
Glioblastoma
5/98 5%
0/0 0%
Chordoma
0/7 0%
1/13 8%
Gastrointestinal Stromal Tumour
0/0 0%
6/133 5%
Melanoma
23/210 11%
57/1899 3%
Non-Small Cell Lung Carcinoma
52/304 17%
5/1390 0%
Hodgkins Lymphoma
3/16 19%
1/122 1%
Unknown
0/10 0%
1/29 3%
Germ Cell Tumour
2/25 8%
2/169 1%
Neuroendocrine Tumour
10/154 6%
5/577 1%
Biliary Tract Carcinoma
3/54 6%
17/950 2%
Endometrial Carcinoma
9/42 21%
3/612 0%
Retinoblastoma
0/27 0%
1/30 3%
Gastric Carcinoma
6/74 8%
25/1809 1%
Colorectal Carcinoma
25/143 17%
30/3239 1%
Ewings Sarcoma
5/63 8%
0/262 0%
Esophageal Squamous Cell Carcinoma
9/51 18%
31/2550 1%
Cervical Carcinoma
3/35 9%
4/422 1%
Other Solid Cancers
8/94 9%
16/1515 1%
Other Sarcomas
6/69 9%
5/699 1%
Ovarian Carcinoma
8/109 7%
6/998 1%
Hepatocellular Carcinoma
2/46 4%
24/2210 1%
Squamous Cell Lung Carcinoma
8/57 14%
2/810 0%
Chondrosarcoma
0/14 0%
1/75 1%
Small Cell Lung Carcinoma
2/9 22%
6/752 1%
Esophageal Carcinoma
2/23 9%
5/769 1%

Mutation Distribution

Where TDRD15 is mutated · all tissues, split by cell line vs tissue

Mutation counts by tissue
Mutation Distribution

How many mutations in TDRD15 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 11 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 1,220 mutations in TDRD15

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