RIPPLY1

Ripply transcriptional repressor 1 Q0D2K3 RIPP1_HUMAN
Protein Coding Chr X Xq22.3 Swiss-Prot reviewed Entrez 92129
Mutations
101
CL 18 · Tissue 83
Samples
67
CL 14 · Tissue 53
Peptides
62
unique mutant peptides
Transcripts
2
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
Mutations1011883
Samples671453
Peptides621252

Function

RIPPLY1 · Ripply transcriptional repressor 1

This gene encodes a protein similar to a zebrafish protein which acts as a transcriptional repressor in and is required for somite segmentation in zebrafish embryos (PMID: 16326386). Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Aug 2011].

Isoforms & Proteins

2 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
ENST00000276173 Q0D2K3 67 51
ENST00000411805 Q0D2K3-2 34 30

Gene Properties

Type
Protein Coding
Chromosome
X
Cytoband
Xq22.3
Entrez ID

Recurrent Mutations

All 51 amino-acid changes on canonical ENST00000276173 · 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 RIPPLY1 · 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 RIPPLY1 – 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
1/42 2%
11/612 2%
Melanoma
4/210 2%
10/1899 1%
Mesothelioma
1/62 2%
0/165 0%
Small Cell Lung Carcinoma
0/9 0%
3/752 0%
Kidney Carcinoma
4/85 5%
1/1862 0%
Head and Neck Carcinoma
0/85 0%
4/1574 0%
Thyroid Gland Carcinoma
0/45 0%
4/1592 0%
Squamous Cell Lung Carcinoma
0/57 0%
2/810 0%
Cervical Carcinoma
1/35 3%
0/422 0%
Other Solid Cancers
0/94 0%
3/1515 0%
Colorectal Carcinoma
0/143 0%
5/3239 0%
Pancreatic Carcinoma
0/89 0%
2/1611 0%
Non-Cancerous
0/104 0%
1/830 0%
Bladder Carcinoma
0/58 0%
1/956 0%
Prostate Carcinoma
2/13 15%
0/2105 0%
Non-Small Cell Lung Carcinoma
0/304 0%
1/1390 0%
Breast Carcinoma
0/144 0%
2/3264 0%
Gastric Carcinoma
0/74 0%
1/1809 0%
B-Cell Non-Hodgkins Lymphoma
0/88 0%
1/2534 0%
B-Lymphoblastic Leukemia
1/55 2%
0/2640 0%
Hepatocellular Carcinoma
0/46 0%
1/2210 0%

Mutation Distribution

Where RIPPLY1 is mutated · all tissues, split by cell line vs tissue

Mutation counts by tissue
Mutation Distribution

How many mutations in RIPPLY1 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 47 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 101 mutations in RIPPLY1

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