LY6E

Lymphocyte antigen 6 family member E Q16553 LY6E_HUMAN
Protein Coding Chr 8 8q24.3 Swiss-Prot reviewed Entrez 4061
Mutations
495
CL 103 · Tissue 377
Samples
77
CL 16 · Tissue 59
Peptides
85
unique mutant peptides
Transcripts
14
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
Mutations495103377
Samples771659
Peptides852361

Function

LY6E · Lymphocyte antigen 6 family member E

This gene belongs to the human Ly6 gene family and encodes a glycosylphosphatidyl-inositol (GPI)-anchored cell surface protein. The protein plays an important role in T cell physiology, oncogenesis and immunological regulation. The protein is also involved in modulation of viral infection by coronaviruses, SARS-CoV, MERS-CoV and SARS-CoV-2. [provided by RefSeq, Aug 2021].

Isoforms & Proteins

14 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
ENST00000292494 Q16553 57 44
ENST00000429120 Q16553 52 43
ENST00000520466 Q16553 52 43
ENST00000521003 Q16553 52 43
ENST00000521699 Q16553 52 43
ENST00000522024 Q16553 52 43
ENST00000522971 Q16553 52 43
ENST00000520531 E5RGI6* 26 21
ENST00000519546 E5RI33* 22 17
ENST00000519611 E5RI33* 22 17
ENST00000523847 E5RIQ1* 19 14
ENST00000521182 E5RI58* 15 11
ENST00000522528 E5RI58* 15 11
ENST00000517503 Q16553 7 3

Gene Properties

Type
Protein Coding
Chromosome
8
Cytoband
8q24.3
Entrez ID
Aliases
RIG-ERIGESCA-2SCA2TSA-1

Recurrent Mutations

All 44 amino-acid changes on canonical ENST00000292494 · 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 LY6E · 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 LY6E – 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
1/40 2%
0/0 0%
Colorectal Carcinoma
6/143 4%
10/3239 0%
Non-Small Cell Lung Carcinoma
3/304 1%
4/1390 0%
Melanoma
0/210 0%
8/1899 0%
Glioma
0/52 0%
7/2127 0%
Ewings Sarcoma
1/63 2%
0/262 0%
Bladder Carcinoma
0/58 0%
3/956 0%
Neuroendocrine Tumour
0/154 0%
2/577 0%
Gastric Carcinoma
0/74 0%
5/1809 0%
Squamous Cell Lung Carcinoma
0/57 0%
2/810 0%
Hepatocellular Carcinoma
0/46 0%
5/2210 0%
Cervical Carcinoma
0/35 0%
1/422 0%
Kidney Carcinoma
0/85 0%
4/1862 0%
Other Solid Cancers
1/94 1%
2/1515 0%
Endometrial Carcinoma
0/42 0%
1/612 0%
Esophageal Squamous Cell Carcinoma
2/51 4%
2/2550 0%
Other Sarcomas
0/69 0%
1/699 0%
B-Lymphoblastic Leukemia
2/55 4%
1/2640 0%
Biliary Tract Carcinoma
0/54 0%
1/950 0%
Pancreatic Carcinoma
0/89 0%
1/1611 0%
Other Blood Cancers
0/61 0%
1/2725 0%

Mutation Distribution

Where LY6E is mutated · all tissues, split by cell line vs tissue

Mutation counts by tissue
Mutation Distribution

How many mutations in LY6E 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 495 mutations in LY6E

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