SLC7A9

Solute carrier family 7 member 9 P82251 BAT1_HUMAN
Protein Coding Chr 19 19q13.11 Swiss-Prot reviewed Entrez 11136
Mutations
1,083
CL 140 · Tissue 924
Samples
362
CL 68 · Tissue 287
Peptides
212
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
Mutations1,083140924
Samples36268287
Peptides21242180

Function

SLC7A9 · Solute carrier family 7 member 9

This gene encodes a protein that belongs to a family of light subunits of amino acid transporters. This protein plays a role in the high-affinity and sodium-independent transport of cystine and neutral and dibasic amino acids, and appears to function in the reabsorption of cystine in the kidney tubule. Mutations in this gene cause non-type I cystinuria, a disease that leads to cystine stones in the urinary system due to impaired transport of cystine and dibasic amino acids. Alternate transcript variants, which encode the same protein, have been found for this gene. [provided by RefSeq, Jul 2011].

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
ENST00000023064 P82251 382 211
ENST00000590341 P82251 351 204
ENST00000587772 P82251 350 203

Gene Properties

Type
Protein Coding
Chromosome
19
Cytoband
19q13.11
Entrez ID
Aliases
BAT1CSNU3

Recurrent Mutations

All 211 amino-acid changes on canonical ENST00000023064 · 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 SLC7A9 · 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 SLC7A9 – 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%
Chronic Myelogenous Leukemia
2/25 8%
0/0 0%
Gastrointestinal Stromal Tumour
0/0 0%
5/133 4%
Endometrial Carcinoma
4/42 10%
20/612 3%
Glioblastoma
3/98 3%
0/0 0%
Melanoma
3/210 1%
48/1899 3%
Oral Cavity Carcinoma
1/54 2%
0/0 0%
Colorectal Carcinoma
12/143 8%
45/3239 1%
Ewings Sarcoma
4/63 6%
1/262 0%
Hodgkins Lymphoma
2/16 12%
0/122 0%
Squamous Cell Lung Carcinoma
2/57 4%
9/810 1%
Non-Cancerous
2/104 2%
9/830 1%
Other Sarcomas
6/69 9%
3/699 0%
Gastric Carcinoma
3/74 4%
17/1809 1%
Bladder Carcinoma
0/58 0%
10/956 1%
Rhabdomyosarcoma
0/33 0%
2/171 1%
Other Solid Cancers
4/94 4%
11/1515 1%
Adrenocortical Carcinoma
0/3 0%
1/112 1%
Non-Small Cell Lung Carcinoma
4/304 1%
10/1390 1%
Esophageal Carcinoma
0/23 0%
5/769 1%
Thyroid Gland Carcinoma
0/45 0%
10/1592 1%
Glioma
0/52 0%
13/2127 1%
Germ Cell Tumour
0/25 0%
1/169 1%
Breast Carcinoma
2/144 1%
15/3264 0%
Biliary Tract Carcinoma
0/54 0%
5/950 1%
Pancreatic Carcinoma
1/89 1%
7/1611 0%
Hepatocellular Carcinoma
0/46 0%
10/2210 0%
Head and Neck Carcinoma
1/85 1%
5/1574 0%
Other Blood Cancers
3/61 5%
5/2725 0%
Ovarian Carcinoma
1/109 1%
2/998 0%

Mutation Distribution

Where SLC7A9 is mutated · all tissues, split by cell line vs tissue

Mutation counts by tissue
Mutation Distribution

How many mutations in SLC7A9 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 1,083 mutations in SLC7A9

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