CRIP1

Cysteine rich protein 1 P50238 CRIP1_HUMAN
Protein Coding Chr 14 14q32.33 Swiss-Prot reviewed Entrez 1396
Mutations
96
CL 27 · Tissue 66
Samples
36
CL 13 · Tissue 22
Peptides
24
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
Mutations962766
Samples361322
Peptides24716

Function

CRIP1 · Cysteine rich protein 1

Cysteine-rich intestinal protein (CRIP) belongs to the LIM/double zinc finger protein family, members of which include cysteine- and glycine-rich protein-1 (CSRP1; MIM 123876), rhombotin-1 (RBTN1; MIM 186921), rhombotin-2 (RBTN2; MIM 180385), and rhombotin-3 (RBTN3; MIM 180386). CRIP may be involved in intestinal zinc transport (Hempe and Cousins, 1991 [PubMed 1946385]).[supplied by OMIM, Mar 2008].

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
ENST00000392531 P50238 35 24
ENST00000409393 P50238 31 22
ENST00000330233 P50238 30 22

Gene Properties

Type
Protein Coding
Chromosome
14
Cytoband
14q32.33
Entrez ID
Aliases
CRHPCRIPCRP-1CRP1

Recurrent Mutations

All 24 amino-acid changes on canonical ENST00000392531 · 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 CRIP1 · 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 CRIP1 – 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
Chronic Myelogenous Leukemia
2/25 8%
0/0 0%
Gastrointestinal Stromal Tumour
0/0 0%
2/133 2%
Endometrial Carcinoma
2/42 5%
0/612 0%
Gastric Carcinoma
0/74 0%
5/1809 0%
Non-Small Cell Lung Carcinoma
3/304 1%
1/1390 0%
Medulloblastoma
0/0 0%
1/450 0%
Melanoma
0/210 0%
3/1899 0%
Esophageal Carcinoma
0/23 0%
1/769 0%
Small Cell Lung Carcinoma
0/9 0%
1/752 0%
Breast Carcinoma
3/144 2%
1/3264 0%
Thyroid Gland Carcinoma
0/45 0%
2/1592 0%
Bladder Carcinoma
1/58 2%
0/956 0%
B-Cell Non-Hodgkins Lymphoma
1/88 1%
1/2534 0%
Other Blood Cancers
0/61 0%
2/2725 0%
Glioma
0/52 0%
1/2127 0%
Hepatocellular Carcinoma
0/46 0%
1/2210 0%
Esophageal Squamous Cell Carcinoma
1/51 2%
0/2550 0%
Colorectal Carcinoma
0/143 0%
1/3239 0%

Mutation Distribution

Where CRIP1 is mutated · all tissues, split by cell line vs tissue

Mutation counts by tissue
Mutation Distribution

How many mutations in CRIP1 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 96 mutations in CRIP1

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