AXL

AXL receptor tyrosine kinase P30530 UFO_HUMAN
Protein Coding Chr 19 19q13.2 Swiss-Prot reviewed Entrez 558
Mutations
1,672
CL 251 · Tissue 1,413
Samples
605
CL 123 · Tissue 478
Peptides
457
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
Mutations1,6722511,413
Samples605123478
Peptides45784390

Function

AXL · AXL receptor tyrosine kinase

The protein encoded by this gene is a member of the Tyro3-Axl-Mer (TAM) receptor tyrosine kinase subfamily. The encoded protein possesses an extracellular domain which is composed of two immunoglobulin-like motifs at the N-terminal, followed by two fibronectin type-III motifs. It transduces signals from the extracellular matrix into the cytoplasm by binding to the vitamin K-dependent protein growth arrest-specific 6 (Gas6). This gene may be involved in several cellular functions including growth, migration, aggregation and anti-inflammation in multiple cell types. The encoded protein acts as a host cell receptor for multiple viruses, including Marburg, Ebola and Lassa viruses and is a candidate receptor for the SARS-CoV2 virus. [provided by RefSeq, Sep 2021].

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
ENST00000301178 P30530 661 439
ENST00000359092 P30530-2 589 413
ENST00000593513 M0R0W6* 422 299

Gene Properties

Type
Protein Coding
Chromosome
19
Cytoband
19q13.2
Entrez ID
Aliases
ARKAXL3JTK11Tyro7UFO

Recurrent Mutations

All 439 amino-acid changes on canonical ENST00000301178 · 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 AXL · 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 AXL – 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
8/40 20%
0/0 0%
Melanoma
11/210 5%
109/1899 6%
Endometrial Carcinoma
4/42 10%
29/612 5%
T-Cell Non-Hodgkins Lymphoma
1/26 4%
0/0 0%
Acute Myeloid Leukemia
3/90 3%
0/0 0%
Hodgkins Lymphoma
2/16 12%
2/122 2%
Colorectal Carcinoma
29/143 20%
63/3239 2%
Unknown
0/10 0%
1/29 3%
Gastric Carcinoma
1/74 1%
40/1809 2%
Other Solid Cancers
7/94 7%
22/1515 1%
Mesothelioma
3/62 5%
1/165 1%
Germ Cell Tumour
1/25 4%
2/169 1%
Neuroendocrine Tumour
9/154 6%
2/577 0%
Pheochromocytoma and Paraganglioma
0/0 0%
1/71 1%
Squamous Cell Lung Carcinoma
1/57 2%
10/810 1%
Non-Small Cell Lung Carcinoma
11/304 4%
9/1390 1%
Bladder Carcinoma
1/58 2%
11/956 1%
Plasma Cell Myeloma
3/44 7%
1/305 0%
Hepatocellular Carcinoma
2/46 4%
22/2210 1%
Thyroid Gland Carcinoma
1/45 2%
16/1592 1%
Other Sarcomas
0/69 0%
7/699 1%
Ovarian Carcinoma
5/109 5%
5/998 0%
Burkitts Lymphoma
2/32 6%
0/196 0%
Non-Cancerous
1/104 1%
7/830 1%
Pancreatic Carcinoma
2/89 2%
11/1611 1%
Prostate Carcinoma
2/13 15%
14/2105 1%
Neuroblastoma
2/87 2%
8/1331 1%
Cervical Carcinoma
0/35 0%
3/422 1%
Small Cell Lung Carcinoma
0/9 0%
5/752 1%
Esophageal Squamous Cell Carcinoma
1/51 2%
15/2550 1%

Mutation Distribution

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

Mutation counts by tissue
Mutation Distribution

How many mutations in AXL 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 1,672 mutations in AXL

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