RBP7

Retinol binding protein 7 Q96R05 RET7_HUMAN
Protein Coding Chr 1 1p36.22 Swiss-Prot reviewed Entrez 116362
Mutations
53
CL 14 · Tissue 39
Samples
53
CL 14 · Tissue 39
Peptides
44
unique mutant peptides
Transcripts
1
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
Mutations531439
Samples531439
Peptides44738

Function

RBP7 · Retinol binding protein 7

The protein encoded by this gene is a member of the cellular retinol-binding protein (CRBP) family, whose members are required for vitamin A stability and metabolism. The encoded protein binds all-trans-retinol and is structurally similar to other CRBPs; however, it has a lower binding affinity for retinol than other CRBPs. [provided by RefSeq, Aug 2016].

Isoforms & Proteins

1 transcript · 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
ENST00000294435 Q96R05 53 44

Gene Properties

Type
Protein Coding
Chromosome
1
Cytoband
1p36.22
Entrez ID
Aliases
CRABP4CRBP4CRBPIV

Recurrent Mutations

All 44 amino-acid changes on canonical ENST00000294435 · 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 RBP7 · 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 RBP7 – 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
Hodgkins Lymphoma
2/16 12%
0/122 0%
Melanoma
2/210 1%
9/1899 0%
Endometrial Carcinoma
2/42 5%
1/612 0%
Non-Small Cell Lung Carcinoma
3/304 1%
2/1390 0%
Other Solid Cancers
2/94 2%
2/1515 0%
Squamous Cell Lung Carcinoma
2/57 4%
0/810 0%
Colorectal Carcinoma
0/143 0%
7/3239 0%
Hepatocellular Carcinoma
0/46 0%
4/2210 0%
Gastric Carcinoma
0/74 0%
3/1809 0%
Other Sarcomas
0/69 0%
1/699 0%
Esophageal Carcinoma
0/23 0%
1/769 0%
Esophageal Squamous Cell Carcinoma
0/51 0%
3/2550 0%
Ovarian Carcinoma
1/109 1%
0/998 0%
Head and Neck Carcinoma
0/85 0%
1/1574 0%
Pancreatic Carcinoma
0/89 0%
1/1611 0%
Kidney Carcinoma
0/85 0%
1/1862 0%
Prostate Carcinoma
0/13 0%
1/2105 0%
Other Blood Cancers
0/61 0%
1/2725 0%
Breast Carcinoma
0/144 0%
1/3264 0%

Mutation Distribution

Where RBP7 is mutated · all tissues, split by cell line vs tissue

Mutation counts by tissue
Mutation Distribution

How many mutations in RBP7 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 53 mutations in RBP7

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