LYPD6B

LY6/PLAUR domain containing 6B Q8NI32 LPD6B_HUMAN
Protein Coding Chr 2 2q23.2 Swiss-Prot reviewed Entrez 130576
Mutations
463
CL 62 · Tissue 396
Samples
132
CL 25 · Tissue 105
Peptides
103
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
Mutations46362396
Samples13225105
Peptides1031988

Function

LYPD6B · LY6/PLAUR domain containing 6B

Enables acetylcholine receptor regulator activity. Predicted to be located in extracellular region and plasma membrane. [provided by Alliance of Genome Resources, Apr 2022]

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
ENST00000409642 Q8NI32-2 127 84
ENST00000280115 H7BXI7* 109 75
ENST00000409876 Q8NI32 109 75
ENST00000409029 Q8NI32 108 74
ENST00000450639 F8WCH4* 10 9

Gene Properties

Type
Protein Coding
Chromosome
2
Cytoband
2q23.2
Entrez ID
Aliases
CT116LYPD7

Recurrent Mutations

All 84 amino-acid changes on canonical ENST00000409642 · 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 LYPD6B · 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 LYPD6B – 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
Endometrial Carcinoma
3/42 7%
16/612 3%
Acute Myeloid Leukemia
1/90 1%
0/0 0%
Melanoma
4/210 2%
11/1899 1%
Colorectal Carcinoma
6/143 4%
17/3239 1%
Neuroendocrine Tumour
4/154 3%
0/577 0%
Gastric Carcinoma
0/74 0%
10/1809 1%
Burkitts Lymphoma
1/32 3%
0/196 0%
Small Cell Lung Carcinoma
0/9 0%
3/752 0%
Non-Small Cell Lung Carcinoma
0/304 0%
6/1390 0%
Bladder Carcinoma
0/58 0%
3/956 0%
Plasma Cell Myeloma
0/44 0%
1/305 0%
Other Sarcomas
1/69 1%
1/699 0%
Esophageal Carcinoma
0/23 0%
2/769 0%
Glioma
0/52 0%
5/2127 0%
Squamous Cell Lung Carcinoma
0/57 0%
2/810 0%
Cervical Carcinoma
0/35 0%
1/422 0%
Medulloblastoma
0/0 0%
1/450 0%
Non-Cancerous
0/104 0%
2/830 0%
Biliary Tract Carcinoma
0/54 0%
2/950 0%
B-Cell Non-Hodgkins Lymphoma
2/88 2%
3/2534 0%
Head and Neck Carcinoma
0/85 0%
3/1574 0%
Ovarian Carcinoma
0/109 0%
2/998 0%
Breast Carcinoma
0/144 0%
5/3264 0%
Hepatocellular Carcinoma
0/46 0%
3/2210 0%
Other Solid Cancers
1/94 1%
1/1515 0%
Kidney Carcinoma
0/85 0%
2/1862 0%
Esophageal Squamous Cell Carcinoma
0/51 0%
2/2550 0%
B-Lymphoblastic Leukemia
2/55 4%
0/2640 0%
Neuroblastoma
0/87 0%
1/1331 0%
Prostate Carcinoma
0/13 0%
1/2105 0%

Mutation Distribution

Where LYPD6B is mutated · all tissues, split by cell line vs tissue

Mutation counts by tissue
Mutation Distribution

How many mutations in LYPD6B 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 463 mutations in LYPD6B

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