RAB37

RAB37, member RAS oncogene family Q96AX2 RAB37_HUMAN
Protein Coding Chr 17 17q25.1 Swiss-Prot reviewed Entrez 326624
Mutations
785
CL 75 · Tissue 700
Samples
158
CL 23 · Tissue 132
Peptides
174
unique mutant peptides
Transcripts
9
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
Mutations78575700
Samples15823132
Peptides17424153

Function

RAB37 · RAB37, member RAS oncogene family

Rab proteins are low molecular mass GTPases that are critical regulators of vesicle trafficking. For additional background information on Rab proteins, see MIM 179508.[supplied by OMIM, Apr 2006].

Isoforms & Proteins

9 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
ENST00000392613 Q96AX2 138 104
ENST00000402449 Q96AX2-2 130 106
ENST00000613645 Q96AX2 113 91
ENST00000528438 B7Z3L0* 105 83
ENST00000340415 A8MSP2* 98 80
ENST00000392612 Q96AX2-4 98 82
ENST00000392610 A8MTC6* 95 75
ENST00000392614 A0A9H3ZVF6* 6 3
ENST00000392615 A8MZI4* 2 2

Gene Properties

Type
Protein Coding
Chromosome
17
Cytoband
17q25.1
Entrez ID

Recurrent Mutations

All 104 amino-acid changes on canonical ENST00000392613 · 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 RAB37 · 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 RAB37 – 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
T-Lymphoblastic Leukemia
1/40 2%
0/0 0%
Oral Cavity Carcinoma
1/54 2%
0/0 0%
Endometrial Carcinoma
2/42 5%
7/612 1%
Melanoma
1/210 0%
24/1899 1%
Acute Myeloid Leukemia
1/90 1%
0/0 0%
Colorectal Carcinoma
1/143 1%
23/3239 1%
Gastric Carcinoma
0/74 0%
12/1809 1%
Ovarian Carcinoma
3/109 3%
4/998 0%
Squamous Cell Lung Carcinoma
3/57 5%
2/810 0%
Small Cell Lung Carcinoma
0/9 0%
4/752 1%
Non-Small Cell Lung Carcinoma
2/304 1%
6/1390 0%
Hepatocellular Carcinoma
2/46 4%
8/2210 0%
Neuroendocrine Tumour
2/154 1%
1/577 0%
Other Solid Cancers
0/94 0%
6/1515 0%
Head and Neck Carcinoma
0/85 0%
6/1574 0%
Ewings Sarcoma
0/63 0%
1/262 0%
Bladder Carcinoma
0/58 0%
3/956 0%
Plasma Cell Myeloma
0/44 0%
1/305 0%
B-Cell Non-Hodgkins Lymphoma
2/88 2%
4/2534 0%
Medulloblastoma
0/0 0%
1/450 0%
Cervical Carcinoma
0/35 0%
1/422 0%
Prostate Carcinoma
0/13 0%
4/2105 0%
Glioma
0/52 0%
4/2127 0%
Kidney Carcinoma
0/85 0%
3/1862 0%
Breast Carcinoma
0/144 0%
4/3264 0%
Non-Cancerous
0/104 0%
1/830 0%
Biliary Tract Carcinoma
0/54 0%
1/950 0%
B-Lymphoblastic Leukemia
2/55 4%
0/2640 0%
Neuroblastoma
0/87 0%
1/1331 0%
Pancreatic Carcinoma
0/89 0%
1/1611 0%

Mutation Distribution

Where RAB37 is mutated · all tissues, split by cell line vs tissue

Mutation counts by tissue
Mutation Distribution

How many mutations in RAB37 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 785 mutations in RAB37

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