SCIMP

SLP adaptor and CSK interacting membrane protein Q6UWF3 SCIMP_HUMAN
Protein Coding Chr 17 17p13.2 Swiss-Prot reviewed Entrez 388325
Mutations
134
CL 19 · Tissue 114
Samples
47
CL 9 · Tissue 37
Peptides
47
unique mutant peptides
Transcripts
4
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
Mutations13419114
Samples47937
Peptides47641

Function

SCIMP · SLP adaptor and CSK interacting membrane protein

This gene encodes a transmembrane adaptor protein that is expressed in antigen-presenting cells and is localized in the immunologic synapse. The encoded protein is involved in major histocompatibility complex class II signal transduction and immune synapse formation. Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Dec 2012].

Isoforms & Proteins

4 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
ENST00000574081 Q6UWF3 45 38
ENST00000399600 Q6UWF3-3 39 35
ENST00000574297 I3L1W2* 26 21
ENST00000571800 Q6UWF3-2 24 20

Gene Properties

Type
Protein Coding
Chromosome
17
Cytoband
17p13.2
Entrez ID
Aliases
C17orf87UNQ5783

Recurrent Mutations

All 38 amino-acid changes on canonical ENST00000574081 · 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 SCIMP · 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 SCIMP – 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
0/42 0%
2/612 0%
Non-Small Cell Lung Carcinoma
1/304 0%
4/1390 0%
Neuroendocrine Tumour
1/154 1%
1/577 0%
Head and Neck Carcinoma
2/85 2%
2/1574 0%
Bladder Carcinoma
1/58 2%
1/956 0%
Colorectal Carcinoma
1/143 1%
5/3239 0%
Ovarian Carcinoma
0/109 0%
2/998 0%
Thyroid Gland Carcinoma
0/45 0%
3/1592 0%
Melanoma
1/210 0%
2/1899 0%
Small Cell Lung Carcinoma
0/9 0%
1/752 0%
Other Sarcomas
0/69 0%
1/699 0%
Other Solid Cancers
0/94 0%
2/1515 0%
Non-Cancerous
0/104 0%
1/830 0%
Biliary Tract Carcinoma
1/54 2%
0/950 0%
Glioma
0/52 0%
2/2127 0%
B-Cell Non-Hodgkins Lymphoma
0/88 0%
2/2534 0%
Esophageal Squamous Cell Carcinoma
1/51 2%
1/2550 0%
Other Blood Cancers
0/61 0%
2/2725 0%
Pancreatic Carcinoma
0/89 0%
1/1611 0%
Gastric Carcinoma
0/74 0%
1/1809 0%
Hepatocellular Carcinoma
0/46 0%
1/2210 0%
B-Lymphoblastic Leukemia
0/55 0%
1/2640 0%

Mutation Distribution

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

Mutation counts by tissue
Mutation Distribution

How many mutations in SCIMP 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 134 mutations in SCIMP

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