RASGRP4

RAS guanyl releasing protein 4 Q8TDF6 GRP4_HUMAN
Protein Coding Chr 19 19q13.2 Swiss-Prot reviewed Entrez 115727
Mutations
2,693
CL 412 · Tissue 2,267
Samples
378
CL 87 · Tissue 288
Peptides
393
unique mutant peptides
Transcripts
8
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
Mutations2,6934122,267
Samples37887288
Peptides39377332

Function

RASGRP4 · RAS guanyl releasing protein 4

The protein encoded by this gene is a member of the Ras guanyl nucleotide-releasing protein (RasGRP) family of Ras guanine nucleotide exchange factors. It contains a Ras exchange motif, a diacylglycerol-binding domain, and two calcium-binding EF hands. This protein was shown to activate H-Ras in a cation-dependent manner in vitro. Expression of this protein in myeloid cell lines was found to be correlated with elevated level of activated RAS protein, and the RAS activation can be greatly enhanced by phorbol ester treatment, which suggested a role of this protein in diacylglycerol regulated cell signaling pathways. Studies of a mast cell leukemia cell line expressing substantial amounts of abnormal transcripts of this gene indicated that this gene may play an important role in the final stages of mast cell development. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Apr 2009].

Isoforms & Proteins

8 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
ENST00000615439 Q8TDF6 417 290
ENST00000454404 Q8TDF6-8 367 260
ENST00000586305 Q8TDF6-2 360 255
ENST00000587738 Q8TDF6 343 246
ENST00000617966 Q8TDF6-7 325 227
ENST00000587753 Q8TDF6-9 316 236
ENST00000614135 Q8TDF6-5 299 222
ENST00000622174 Q8TDF6-6 266 193

Gene Properties

Type
Protein Coding
Chromosome
19
Cytoband
19q13.2
Entrez ID

Recurrent Mutations

All 290 amino-acid changes on canonical ENST00000615439 · 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 RASGRP4 · 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 RASGRP4 – 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%
T-Lymphoblastic Leukemia
2/40 5%
0/0 0%
Gastrointestinal Stromal Tumour
0/0 0%
6/133 5%
Oral Cavity Carcinoma
2/54 4%
0/0 0%
Chondrosarcoma
2/14 14%
1/75 1%
Endometrial Carcinoma
4/42 10%
15/612 2%
Melanoma
7/210 3%
41/1899 2%
Acute Myeloid Leukemia
2/90 2%
0/0 0%
Cervical Carcinoma
0/35 0%
7/422 2%
Osteosarcoma
3/45 7%
0/166 0%
Pheochromocytoma and Paraganglioma
0/0 0%
1/71 1%
Non-Small Cell Lung Carcinoma
7/304 2%
15/1390 1%
Squamous Cell Lung Carcinoma
0/57 0%
11/810 1%
Gastric Carcinoma
3/74 4%
19/1809 1%
Glioblastoma
1/98 1%
0/0 0%
Hepatocellular Carcinoma
3/46 7%
19/2210 1%
Colorectal Carcinoma
8/143 6%
24/3239 1%
Other Solid Cancers
1/94 1%
14/1515 1%
Esophageal Squamous Cell Carcinoma
0/51 0%
23/2550 1%
Mesothelioma
2/62 3%
0/165 0%
Plasma Cell Myeloma
1/44 2%
2/305 1%
Hodgkins Lymphoma
0/16 0%
1/122 1%
Biliary Tract Carcinoma
2/54 4%
5/950 1%
Bladder Carcinoma
2/58 3%
5/956 1%
Thyroid Gland Carcinoma
3/45 7%
7/1592 0%
Small Cell Lung Carcinoma
0/9 0%
4/752 1%
Other Sarcomas
3/69 4%
1/699 0%
Germ Cell Tumour
0/25 0%
1/169 1%
Kidney Carcinoma
3/85 4%
7/1862 0%
Esophageal Carcinoma
0/23 0%
4/769 1%

Mutation Distribution

Where RASGRP4 is mutated · all tissues, split by cell line vs tissue

Mutation counts by tissue
Mutation Distribution

How many mutations in RASGRP4 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 2,693 mutations in RASGRP4

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