RAB14

RAB14, member RAS oncogene family P61106 RAB14_HUMAN
Protein Coding Chr 9 9q33.2 Swiss-Prot reviewed Entrez 51552
Mutations
81
CL 22 · Tissue 57
Samples
78
CL 22 · Tissue 55
Peptides
62
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
Mutations812257
Samples782255
Peptides621349

Function

RAB14 · RAB14, member RAS oncogene family

RAB14 belongs to the large RAB family of low molecular mass GTPases that are involved in intracellular membrane trafficking. These proteins act as molecular switches that flip between an inactive GDP-bound state and an active GTP-bound state in which they recruit downstream effector proteins onto membranes (Junutula et al., 2004 [PubMed 15004230]).[supplied by OMIM, Mar 2009].

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
ENST00000373840 P61106 81 62

Gene Properties

Type
Protein Coding
Chromosome
9
Cytoband
9q33.2
Entrez ID
Aliases
FBPRAB-14

Recurrent Mutations

All 62 amino-acid changes on canonical ENST00000373840 · 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 RAB14 · 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 RAB14 – 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
6/40 15%
0/0 0%
Unknown
1/10 10%
0/29 0%
Endometrial Carcinoma
2/42 5%
4/612 1%
Gastric Carcinoma
4/74 5%
6/1809 0%
Osteosarcoma
0/45 0%
1/166 1%
Burkitts Lymphoma
0/32 0%
1/196 1%
Meningioma
0/3 0%
1/252 0%
Melanoma
2/210 1%
6/1899 0%
Colorectal Carcinoma
0/143 0%
10/3239 0%
Neuroendocrine Tumour
2/154 1%
0/577 0%
Hepatocellular Carcinoma
0/46 0%
6/2210 0%
Ovarian Carcinoma
1/109 1%
2/998 0%
Cervical Carcinoma
0/35 0%
1/422 0%
Wilms Tumour
0/5 0%
1/474 0%
Other Solid Cancers
1/94 1%
2/1515 0%
Glioma
0/52 0%
4/2127 0%
Prostate Carcinoma
0/13 0%
3/2105 0%
Small Cell Lung Carcinoma
0/9 0%
1/752 0%
Squamous Cell Lung Carcinoma
1/57 2%
0/810 0%
Breast Carcinoma
0/144 0%
4/3264 0%
Non-Cancerous
1/104 1%
0/830 0%
B-Cell Non-Hodgkins Lymphoma
0/88 0%
2/2534 0%
Kidney Carcinoma
1/85 1%
0/1862 0%
Esophageal Squamous Cell Carcinoma
0/51 0%
1/2550 0%

Mutation Distribution

Where RAB14 is mutated · all tissues, split by cell line vs tissue

Mutation counts by tissue
Mutation Distribution

How many mutations in RAB14 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 81 mutations in RAB14

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