SPHK1

Sphingosine kinase 1 Q9NYA1 SPHK1_HUMAN
Protein Coding Chr 17 17q25.1 Swiss-Prot reviewed Entrez 8877
Mutations
875
CL 144 · Tissue 724
Samples
218
CL 42 · Tissue 173
Peptides
154
unique mutant peptides
Transcripts
5
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
Mutations875144724
Samples21842173
Peptides15425132

Function

SPHK1 · Sphingosine kinase 1

The protein encoded by this gene catalyzes the phosphorylation of sphingosine to form sphingosine-1-phosphate (S1P), a lipid mediator with both intra- and extracellular functions. Intracellularly, S1P regulates proliferation and survival, and extracellularly, it is a ligand for cell surface G protein-coupled receptors. This protein, and its product S1P, play a key role in TNF-alpha signaling and the NF-kappa-B activation pathway important in inflammatory, antiapoptotic, and immune processes. Phosphorylation of this protein alters its catalytic activity and promotes its translocation to the plasma membrane. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Sep 2017].

Isoforms & Proteins

5 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
ENST00000323374 Q9NYA1-2 217 142
ENST00000592299 Q9NYA1 178 132
ENST00000590959 Q9NYA1-3 162 128
ENST00000392496 Q9NYA1 159 125
ENST00000545180 Q9NYA1 159 125

Gene Properties

Type
Protein Coding
Chromosome
17
Cytoband
17q25.1
Entrez ID
Aliases
SPHK

Recurrent Mutations

All 142 amino-acid changes on canonical ENST00000323374 · 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 SPHK1 · 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 SPHK1 – 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
2/40 5%
0/0 0%
Acute Monocytic Leukemia
0/1 0%
1/25 4%
Gastrointestinal Stromal Tumour
0/0 0%
4/133 3%
Endometrial Carcinoma
7/42 17%
9/612 1%
Burkitts Lymphoma
3/32 9%
0/196 0%
Melanoma
2/210 1%
22/1899 1%
Acute Myeloid Leukemia
1/90 1%
0/0 0%
Colorectal Carcinoma
5/143 4%
30/3239 1%
Glioblastoma
1/98 1%
0/0 0%
Osteosarcoma
1/45 2%
1/166 1%
Gastric Carcinoma
2/74 3%
14/1809 1%
Ovarian Carcinoma
1/109 1%
7/998 1%
Bladder Carcinoma
0/58 0%
7/956 1%
Esophageal Carcinoma
0/23 0%
5/769 1%
Squamous Cell Lung Carcinoma
0/57 0%
5/810 1%
Plasma Cell Myeloma
2/44 5%
0/305 0%
Hepatocellular Carcinoma
2/46 4%
9/2210 0%
Thyroid Gland Carcinoma
0/45 0%
8/1592 0%
Mesothelioma
1/62 2%
0/165 0%
Cervical Carcinoma
0/35 0%
2/422 0%
Esophageal Squamous Cell Carcinoma
3/51 6%
7/2550 0%
Glioma
0/52 0%
8/2127 0%
Pancreatic Carcinoma
1/89 1%
5/1611 0%
Kidney Carcinoma
1/85 1%
5/1862 0%
Other Solid Cancers
0/94 0%
5/1515 0%
Biliary Tract Carcinoma
0/54 0%
3/950 0%
Non-Small Cell Lung Carcinoma
2/304 1%
3/1390 0%
Other Sarcomas
0/69 0%
2/699 0%
Head and Neck Carcinoma
1/85 1%
3/1574 0%
Medulloblastoma
0/0 0%
1/450 0%

Mutation Distribution

Where SPHK1 is mutated · all tissues, split by cell line vs tissue

Mutation counts by tissue
Mutation Distribution

How many mutations in SPHK1 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 875 mutations in SPHK1

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