CCDC144A

Coiled-coil domain containing 144A A2RUR9 C144A_HUMAN
Protein Coding Chr 17 17p11.2 Swiss-Prot reviewed Entrez 9720
Mutations
1,120
CL 86 · Tissue 1,030
Samples
386
CL 35 · Tissue 349
Peptides
354
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
Mutations1,120861,030
Samples38635349
Peptides35436323

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
ENST00000399273 C9JT67* 446 342
ENST00000360524 A2RUR9 440 338
ENST00000340621 A6NJB5* 234 185

Gene Properties

Type
Protein Coding
Chromosome
17
Cytoband
17p11.2
Entrez ID

Recurrent Mutations

All 338 amino-acid changes on canonical ENST00000360524 · 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 CCDC144A · 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 CCDC144A – 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
3/40 8%
0/0 0%
Endometrial Carcinoma
0/42 0%
39/612 6%
T-Cell Non-Hodgkins Lymphoma
1/26 4%
0/0 0%
Melanoma
3/210 1%
60/1899 3%
Unknown
0/10 0%
1/29 3%
Gastrointestinal Stromal Tumour
0/0 0%
3/133 2%
Oral Cavity Carcinoma
1/54 2%
0/0 0%
Cervical Carcinoma
0/35 0%
8/422 2%
Other Solid Cancers
3/94 3%
24/1515 2%
Neuroendocrine Tumour
4/154 3%
7/577 1%
Bladder Carcinoma
1/58 2%
12/956 1%
Colorectal Carcinoma
4/143 3%
37/3239 1%
Chondrosarcoma
0/14 0%
1/75 1%
Gastric Carcinoma
1/74 1%
20/1809 1%
Acute Myeloid Leukemia
1/90 1%
0/0 0%
Glioblastoma
1/98 1%
0/0 0%
Non-Small Cell Lung Carcinoma
5/304 2%
11/1390 1%
Thyroid Gland Carcinoma
1/45 2%
14/1592 1%
Esophageal Carcinoma
0/23 0%
6/769 1%
Hodgkins Lymphoma
1/16 6%
0/122 0%
Small Cell Lung Carcinoma
0/9 0%
5/752 1%
Hepatocellular Carcinoma
1/46 2%
14/2210 1%
Esophageal Squamous Cell Carcinoma
2/51 4%
15/2550 1%
Breast Carcinoma
0/144 0%
21/3264 1%
Squamous Cell Lung Carcinoma
1/57 2%
4/810 0%
B-Cell Non-Hodgkins Lymphoma
0/88 0%
11/2534 0%
Kidney Carcinoma
0/85 0%
8/1862 0%
Glioma
0/52 0%
8/2127 0%
Plasma Cell Myeloma
0/44 0%
1/305 0%
Prostate Carcinoma
0/13 0%
5/2105 0%

Mutation Distribution

Where CCDC144A is mutated · all tissues, split by cell line vs tissue

Mutation counts by tissue
Mutation Distribution

How many mutations in CCDC144A 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 1,120 mutations in CCDC144A

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