CALML4

Calmodulin like 4 Q96GE6-2 CALL4_HUMAN
Protein Coding Chr 15 15q23 Swiss-Prot reviewed Entrez 91860
Mutations
67
CL 9 · Tissue 55
Samples
59
CL 9 · Tissue 47
Peptides
51
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
Mutations67955
Samples59947
Peptides51844

Function

CALML4 · Calmodulin like 4

Predicted to enable calcium ion binding activity and enzyme regulator activity. Predicted to be involved in regulation of catalytic activity. [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
ENST00000395463 Q96GE6-2 50 39
ENST00000467889 Q96GE6-6 12 11
ENST00000540479 Q96GE6-3 3 3
ENST00000448060 A0A804D2Q3* 2 2

Gene Properties

Type
Protein Coding
Chromosome
15
Cytoband
15q23
Entrez ID
Aliases
NY-BR-20

Recurrent Mutations

All 39 amino-acid changes on canonical ENST00000395463 · 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 CALML4 · 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 CALML4 – 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
Glioblastoma
1/98 1%
0/0 0%
Gastrointestinal Stromal Tumour
0/0 0%
1/133 1%
Endometrial Carcinoma
0/42 0%
4/612 1%
Melanoma
1/210 0%
6/1899 0%
Colorectal Carcinoma
3/143 2%
8/3239 0%
Ewings Sarcoma
0/63 0%
1/262 0%
Esophageal Carcinoma
0/23 0%
2/769 0%
Other Solid Cancers
0/94 0%
4/1515 0%
Head and Neck Carcinoma
0/85 0%
4/1574 0%
Kidney Carcinoma
0/85 0%
4/1862 0%
Gastric Carcinoma
0/74 0%
3/1809 0%
Other Sarcomas
0/69 0%
1/699 0%
Other Blood Cancers
0/61 0%
3/2725 0%
Bladder Carcinoma
0/58 0%
1/956 0%
Hepatocellular Carcinoma
0/46 0%
2/2210 0%
Breast Carcinoma
2/144 1%
1/3264 0%
Ovarian Carcinoma
0/109 0%
1/998 0%
B-Cell Non-Hodgkins Lymphoma
0/88 0%
2/2534 0%
Thyroid Gland Carcinoma
1/45 2%
0/1592 0%
Non-Small Cell Lung Carcinoma
0/304 0%
1/1390 0%
Prostate Carcinoma
1/13 8%
0/2105 0%
Esophageal Squamous Cell Carcinoma
0/51 0%
1/2550 0%

Mutation Distribution

Where CALML4 is mutated · all tissues, split by cell line vs tissue

Mutation counts by tissue
Mutation Distribution

How many mutations in CALML4 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 67 mutations in CALML4

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