SLC6A2

Solute carrier family 6 member 2 P23975 SC6A2_HUMAN
Protein Coding Chr 16 16q12.2 Swiss-Prot reviewed Entrez 6530
Mutations
2,951
CL 370 · Tissue 2,548
Samples
497
CL 106 · Tissue 384
Peptides
365
unique mutant peptides
Transcripts
7
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
Mutations2,9513702,548
Samples497106384
Peptides36564317

Function

SLC6A2 · Solute carrier family 6 member 2

This gene encodes a member of the sodium:neurotransmitter symporter family. This member is a multi-pass membrane protein, which is responsible for reuptake of norepinephrine into presynaptic nerve terminals and is a regulator of norepinephrine homeostasis. Mutations in this gene cause orthostatic intolerance, a syndrome characterized by lightheadedness, fatigue, altered mentation and syncope. Alternatively spliced transcript variants encoding different isoforms have been identified in this gene.[provided by RefSeq, Feb 2010].

Isoforms & Proteins

7 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
ENST00000568943 P23975 510 309
ENST00000219833 P23975-2 441 294
ENST00000379906 P23975 438 291
ENST00000561820 H3BML6* 422 278
ENST00000566163 H3BRE9* 408 271
ENST00000414754 H3BM11* 391 264
ENST00000567238 P23975-3 341 232

Gene Properties

Type
Protein Coding
Chromosome
16
Cytoband
16q12.2
Entrez ID
Aliases
NAT1NETNET1SLC6A5

Recurrent Mutations

All 309 amino-acid changes on canonical ENST00000568943 · 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 SLC6A2 · 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 SLC6A2 – 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
4/40 10%
0/0 0%
T-Cell Non-Hodgkins Lymphoma
1/26 4%
0/0 0%
Endometrial Carcinoma
6/42 14%
18/612 3%
Glioblastoma
3/98 3%
0/0 0%
Non-Small Cell Lung Carcinoma
17/304 6%
33/1390 2%
Colorectal Carcinoma
23/143 16%
70/3239 2%
Melanoma
7/210 3%
50/1899 3%
Gastric Carcinoma
4/74 5%
38/1809 2%
Squamous Cell Lung Carcinoma
8/57 14%
9/810 1%
Cervical Carcinoma
0/35 0%
8/422 2%
Rhabdomyosarcoma
1/33 3%
2/171 1%
Neuroendocrine Tumour
3/154 2%
6/577 1%
Biliary Tract Carcinoma
3/54 6%
9/950 1%
Ovarian Carcinoma
7/109 6%
6/998 1%
Small Cell Lung Carcinoma
0/9 0%
7/752 1%
Bladder Carcinoma
0/58 0%
9/956 1%
Adrenocortical Carcinoma
0/3 0%
1/112 1%
Other Solid Cancers
2/94 2%
12/1515 1%
Thyroid Gland Carcinoma
1/45 2%
11/1592 1%
Esophageal Carcinoma
3/23 13%
2/769 0%
Hepatocellular Carcinoma
2/46 4%
12/2210 1%
Glioma
0/52 0%
13/2127 1%
Head and Neck Carcinoma
1/85 1%
9/1574 1%
Pancreatic Carcinoma
0/89 0%
9/1611 1%
Germ Cell Tumour
0/25 0%
1/169 1%
Other Sarcomas
3/69 4%
1/699 0%
Esophageal Squamous Cell Carcinoma
1/51 2%
11/2550 0%
Mesothelioma
0/62 0%
1/165 1%
Burkitts Lymphoma
1/32 3%
0/196 0%
Breast Carcinoma
2/144 1%
13/3264 0%

Mutation Distribution

Where SLC6A2 is mutated · all tissues, split by cell line vs tissue

Mutation counts by tissue
Mutation Distribution

How many mutations in SLC6A2 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 46 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 2,951 mutations in SLC6A2

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